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

dbVar

Database of genomic structural variation

nsv6112806

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:543,172

Description:GRCh37/hg19 16p11.2(chr16:29675050-30218221)x1 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: 1923 SVs from 93 studies. See in: genome view

Remapped(Score: Perfect):29,663,729-30,206,900

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Inner Start	Inner Stop
nsv6112806	Remapped	Perfect	GRCh38.p12	Primary Assembly	First Pass	NC_000016.10	Chr16	29,663,729	30,206,900
nsv6112806	Submitted genomic		GRCh37 (hg19)	Primary Assembly		NC_000016.9	Chr16	29,675,050	30,218,221

Variant Call Information

Variant Call ID	Type	Method	Analysis	Subject Phenotype	Clinical Interpretation	Source of Interpretation	ClinVar ID	Copy number
nssv17649966	copy number loss	Multiple	Multiple	not provided	Pathogenic	ClinVar	RCV001532339.9, VCV001176677.10	1

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Inner Start	Inner Stop
nssv17649966	Remapped	Perfect	NC_000016.10:g.(?_ 29663729)_(3020690 0_?)del	GRCh38.p12	First Pass	NC_000016.10	Chr16	29,663,729	30,206,900
nssv17649966	Submitted genomic		NC_000016.9:g.(?_2 9675050)_(30218221 _?)del	GRCh37 (hg19)		NC_000016.9	Chr16	29,675,050	30,218,221

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
nssv17649966	GRCh37: NC_000016.9:g.(?_29675050)_(30218221_?)del	copy number loss	germline	not provided	Pathogenic	ClinVar	RCV001532339.9, VCV001176677.10	1

No genotype data were submitted for this variant

You are here: NCBI