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dbVar

Database of genomic structural variation

nsv6308916

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:3,652,714

Description:NC_000010.10:g.(?_67680088)_(71332799_?)del 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: 13214 SVs from 120 studies. See in: genome view

Remapped(Score: Perfect):65,920,330-69,573,043

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Inner Start	Inner Stop
nsv6308916	Remapped	Perfect	GRCh38.p12	Primary Assembly	First Pass	NC_000010.11	Chr10	65,920,330	69,573,043
nsv6308916	Submitted genomic		GRCh37 (hg19)	Primary Assembly		NC_000010.10	Chr10	67,680,088	71,332,799

Variant Call Information

Variant Call ID	Type	Method	Analysis	Subject Phenotype	Clinical Interpretation	Source of Interpretation	ClinVar ID
nssv17971485	deletion	Multiple	Multiple	not provided	Uncertain significance	ClinVar	RCV001956019.2, VCV001444876.2

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Inner Start	Inner Stop
nssv17971485	Remapped	Perfect	NC_000010.11:g.(?_ 65920330)_(6957304 3_?)del	GRCh38.p12	First Pass	NC_000010.11	Chr10	65,920,330	69,573,043
nssv17971485	Submitted genomic		NC_000010.10:g.(?_ 67680088)_(7133279 9_?)del	GRCh37 (hg19)		NC_000010.10	Chr10	67,680,088	71,332,799

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
nssv17971485	GRCh37: NC_000010.10:g.(?_67680088)_(71332799_?)del	deletion	germline	not provided	Uncertain significance	ClinVar	RCV001956019.2, VCV001444876.2

No genotype data were submitted for this variant

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