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dbVar

Database of genomic structural variation

nsv5836731

Organism: Homo sapiens

Study:nstd209 (Almarri et al. 2020)
Variant Type:copy number variation
Method Type:Sequencing
Submitted on:GRCh38

Variant Calls:2
Validation:Not tested
Clinical Assertions: No
Region Size:2,100

Publication(s):Almarri et al. 2020

Links to Other Resources

Overlapping Genes

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: 130 SVs from 33 studies. See in: genome view

Submitted genomic67,571,951-67,574,050

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5836731	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000003.12	Chr3	67,571,951	67,574,050
nsv5836731	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000003.11	Chr3	67,622,375	67,624,474

Variant Call Information

Variant Call ID	Type	Method	Analysis	Copy number
nssv17494634	copy number variation	Sequencing	Sequence alignment	0
nssv17494635	copy number variation	Sequencing	Sequence alignment	2

Variant Call Placement Information

Variant Call ID	Placement Type	Score	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17494634	Submitted genomic		GRCh38 (hg38)		NC_000003.12	Chr3	67,571,951	67,574,050
nssv17494635	Submitted genomic		GRCh38 (hg38)		NC_000003.12	Chr3	67,571,951	67,574,050
nssv17494634	Remapped	Perfect	GRCh37.p13	First Pass	NC_000003.11	Chr3	67,622,375	67,624,474
nssv17494635	Remapped	Perfect	GRCh37.p13	First Pass	NC_000003.11	Chr3	67,622,375	67,624,474

No validation data were submitted for this variant

No clinical assertion data were submitted for this variant

Genotype and/or allele frequency data can be found on dbVar's FTP site.

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