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dbVar

Database of genomic structural variation

nsv4456351

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:390,805

Description:GRCh37/hg19 6p22.2(chr6:25896585-26287389)x4 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: 1055 SVs from 86 studies. See in: genome view

Remapped(Score: Perfect):25,896,357-26,287,161

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Inner Start	Inner Stop
nsv4456351	Remapped	Perfect	GRCh38.p12	Primary Assembly	First Pass	NC_000006.12	Chr6	25,896,357	26,287,161
nsv4456351	Submitted genomic		GRCh37 (hg19)	Primary Assembly		NC_000006.11	Chr6	25,896,585	26,287,389

Variant Call Information

Variant Call ID	Type	Method	Analysis	Subject Phenotype	Clinical Interpretation	Source of Interpretation	ClinVar ID	Copy number
nssv15774351	copy number gain	Multiple	Multiple	not provided	Uncertain significance	ClinVar	RCV000845790.2, VCV000685082.2	4

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Inner Start	Inner Stop
nssv15774351	Remapped	Perfect	NC_000006.12:g.(?_ 25896357)_(2628716 1_?)dup	GRCh38.p12	First Pass	NC_000006.12	Chr6	25,896,357	26,287,161
nssv15774351	Submitted genomic		NC_000006.11:g.(?_ 25896585)_(2628738 9_?)dup	GRCh37 (hg19)		NC_000006.11	Chr6	25,896,585	26,287,389

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
nssv15774351	GRCh37: NC_000006.11:g.(?_25896585)_(26287389_?)dup	copy number gain	unknown	not provided	Uncertain significance	ClinVar	RCV000845790.2, VCV000685082.2	4

No genotype data were submitted for this variant

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