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

dbVar

Database of genomic structural variation

nsv7093752

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:2,961

Description:NC_000011.9:g.(?_111779488)_(111782448_?)del AND Dilated cardiomyopathy 1II

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: 76 SVs from 18 studies. See in: genome view

Remapped(Score: Perfect):111,908,764-111,911,724

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Inner Start	Inner Stop
nsv7093752	Remapped	Perfect	GRCh38.p12	Primary Assembly	First Pass	NC_000011.10	Chr11	111,908,764	111,911,724
nsv7093752	Submitted genomic		GRCh37 (hg19)	Primary Assembly		NC_000011.9	Chr11	111,779,488	111,782,448

Variant Call Information

Variant Call ID	Type	Method	Analysis	Subject Phenotype	Clinical Interpretation	Source of Interpretation	ClinVar ID
nssv18788214	deletion	Multiple	Multiple	CARDIOMYOPATHY, DILATED, 1II; CMD1II; Dilated cardiomyopathy 1II; Familial isolated dilated cardiomyopathy	Pathogenic	ClinVar	RCV003107530.2, VCV002424297.2

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Inner Start	Inner Stop
nssv18788214	Remapped	Perfect	NC_000011.10:g.(?_ 111908764)_(111911 724_?)del	GRCh38.p12	First Pass	NC_000011.10	Chr11	111,908,764	111,911,724
nssv18788214	Submitted genomic		NC_000011.9:g.(?_1 11779488)_(1117824 48_?)del	GRCh37 (hg19)		NC_000011.9	Chr11	111,779,488	111,782,448

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
nssv18788214	GRCh37: NC_000011.9:g.(?_111779488)_(111782448_?)del	deletion	germline	CARDIOMYOPATHY, DILATED, 1II; CMD1II; Dilated cardiomyopathy 1II; Familial isolated dilated cardiomyopathy	Pathogenic	ClinVar	RCV003107530.2, VCV002424297.2

No genotype data were submitted for this variant

You are here: NCBI