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dbVar

Database of genomic structural variation

nsv4682937

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:30,198

Description:NC_000014.9:g.(?_23390047)_(23420244_?)dup AND Hypertrophic cardiomyopathy

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: 88 SVs from 30 studies. See in: genome view

Remapped(Score: Perfect):23,390,047-23,420,244

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Inner Start	Inner Stop
nsv4682937	Remapped	Perfect	GRCh38.p12	Primary Assembly	First Pass	NC_000014.9	Chr14	23,390,047	23,420,244
nsv4682937	Submitted genomic		GRCh37 (hg19)	Primary Assembly		NC_000014.8	Chr14	23,859,256	23,889,453

Variant Call Information

Variant Call ID	Type	Method	Analysis	Subject Phenotype	Clinical Interpretation	Source of Interpretation	ClinVar ID
nssv16214644	duplication	Multiple	Multiple	Cardiomyopathy, Hypertrophic; Hypertrophic cardiomyopathy; Hypertrophic cardiomyopathy	Uncertain significance	ClinVar	RCV001032471.1, VCV000831948.1

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Inner Start	Inner Stop
nssv16214644	Remapped	Perfect	NC_000014.9:g.(?_2 3390047)_(23420244 _?)dup	GRCh38.p12	First Pass	NC_000014.9	Chr14	23,390,047	23,420,244
nssv16214644	Submitted genomic		NC_000014.8:g.(?_2 3859256)_(23889453 _?)dup	GRCh37 (hg19)		NC_000014.8	Chr14	23,859,256	23,889,453

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
nssv16214644	GRCh37: NC_000014.8:g.(?_23859256)_(23889453_?)dup	duplication	germline	Cardiomyopathy, Hypertrophic; Hypertrophic cardiomyopathy; Hypertrophic cardiomyopathy	Uncertain significance	ClinVar	RCV001032471.1, VCV000831948.1

No genotype data were submitted for this variant

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