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

dbVar

Database of genomic structural variation

nsv7097439

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:36,088

Description:NC_000006.11:g.(?_52869947)_(52906034_?)dup 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: 113 SVs from 29 studies. See in: genome view

Remapped(Score: Perfect):53,005,149-53,041,236

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Inner Start	Inner Stop
nsv7097439	Remapped	Perfect	GRCh38.p12	Primary Assembly	First Pass	NC_000006.12	Chr6	53,005,149	53,041,236
nsv7097439	Submitted genomic		GRCh37 (hg19)	Primary Assembly		NC_000006.11	Chr6	52,869,947	52,906,034

Variant Call Information

Variant Call ID	Type	Method	Analysis	Subject Phenotype	Clinical Interpretation	Source of Interpretation	ClinVar ID
nssv18786833	duplication	Multiple	Multiple	not provided	Uncertain significance	ClinVar	RCV003119746.2, VCV002426307.2

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Inner Start	Inner Stop
nssv18786833	Remapped	Perfect	NC_000006.12:g.(?_ 53005149)_(5304123 6_?)dup	GRCh38.p12	First Pass	NC_000006.12	Chr6	53,005,149	53,041,236
nssv18786833	Submitted genomic		NC_000006.11:g.(?_ 52869947)_(5290603 4_?)dup	GRCh37 (hg19)		NC_000006.11	Chr6	52,869,947	52,906,034

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
nssv18786833	GRCh37: NC_000006.11:g.(?_52869947)_(52906034_?)dup	duplication	germline	not provided	Uncertain significance	ClinVar	RCV003119746.2, VCV002426307.2

No genotype data were submitted for this variant

You are here: NCBI