Warning: The NCBI web site requires JavaScript to function. more...

dbVar

Database of genomic structural variation

nsv4682948

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:4,161,070

Description:NC_000023.10:g.(?_82763333)_(86924394_?)del 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: 6239 SVs from 79 studies. See in: genome view

Remapped(Score: Perfect):83,508,325-87,669,394

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Inner Start	Inner Stop
nsv4682948	Remapped	Perfect	GRCh38.p12	Primary Assembly	First Pass	NC_000023.11	ChrX	83,508,325	87,669,394
nsv4682948	Submitted genomic		GRCh37 (hg19)	Primary Assembly		NC_000023.10	ChrX	82,763,333	86,924,394

Variant Call Information

Variant Call ID	Type	Method	Analysis	Subject Phenotype	Clinical Interpretation	Source of Interpretation	ClinVar ID
nssv16212873	deletion	Multiple	Multiple	not provided	Pathogenic	ClinVar	RCV001033898.1, VCV000833457.1

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Inner Start	Inner Stop
nssv16212873	Remapped	Perfect	NC_000023.11:g.(?_ 83508325)_(8766939 4_?)del	GRCh38.p12	First Pass	NC_000023.11	ChrX	83,508,325	87,669,394
nssv16212873	Submitted genomic		NC_000023.10:g.(?_ 82763333)_(8692439 4_?)del	GRCh37 (hg19)		NC_000023.10	ChrX	82,763,333	86,924,394

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
nssv16212873	GRCh37: NC_000023.10:g.(?_82763333)_(86924394_?)del	deletion	germline	not provided	Pathogenic	ClinVar	RCV001033898.1, VCV000833457.1

No genotype data were submitted for this variant

You are here: NCBI