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dbVar

Database of genomic structural variation

nsv4675970

Organism: Homo sapiens

Study:nstd102 (Clinical Structural Variants)
Variant Type:copy number variation
Method Type:Multiple
Submitted on:GRCh37

Variant Calls:1
Validation:Not tested
Clinical Assertions: Yes
Region Size:7,775,025

Description:GRCh37/hg19 16p12.2-11.2(chr16:21576802-29351826)x3 AND not provided

Links to Other Resources

Source: NCBI

Genome View
Variant Region Details and Evidence
Validation Information
Clinical Assertions
Genotype Information

Genome View

Select assembly:

Overlapping variant regions from other studies: 22708 SVs from 141 studies. See in: genome view

Remapped(Score: Perfect):21,565,481-29,340,505

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Inner Start	Inner Stop
nsv4675970	Remapped	Perfect	GRCh38.p12	Primary Assembly	First Pass	NC_000016.10	Chr16	21,565,481	29,340,505
nsv4675970	Submitted genomic		GRCh37 (hg19)	Primary Assembly		NC_000016.9	Chr16	21,576,802	29,351,826

Variant Call Information

Variant Call ID	Type	Method	Analysis	Subject Phenotype	Clinical Interpretation	Source of Interpretation	ClinVar ID	Copy number
nssv16207267	copy number gain	Multiple	Multiple	not provided	Pathogenic	ClinVar	RCV001006786.2, VCV000815811.2	3

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Inner Start	Inner Stop
nssv16207267	Remapped	Perfect	NC_000016.10:g.(?_ 21565481)_(2934050 5_?)dup	GRCh38.p12	First Pass	NC_000016.10	Chr16	21,565,481	29,340,505
nssv16207267	Submitted genomic		NC_000016.9:g.(?_2 1576802)_(29351826 _?)dup	GRCh37 (hg19)		NC_000016.9	Chr16	21,576,802	29,351,826

No validation data were submitted for this variant

Clinical Assertions

Variant Call ID	HGVS	Type	Allele Origin	Subject Phenotype	Clinical Interpretation	Source of Interpretation	ClinVar ID	Copy number
nssv16207267	GRCh37: NC_000016.9:g.(?_21576802)_(29351826_?)dup	copy number gain	germline	not provided	Pathogenic	ClinVar	RCV001006786.2, VCV000815811.2	3

No genotype data were submitted for this variant

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