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dbVar

Database of genomic structural variation

nsv7097583

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:322,860

Description:NC_000006.11:g.(?_66094259)_(66417118_?)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: 1256 SVs from 102 studies. See in: genome view

Remapped(Score: Perfect):65,384,366-65,707,225

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Inner Start	Inner Stop
nsv7097583	Remapped	Perfect	GRCh38.p12	Primary Assembly	First Pass	NC_000006.12	Chr6	65,384,366	65,707,225
nsv7097583	Submitted genomic		GRCh37 (hg19)	Primary Assembly		NC_000006.11	Chr6	66,094,259	66,417,118

Variant Call Information

Variant Call ID	Type	Method	Analysis	Subject Phenotype	Clinical Interpretation	Source of Interpretation	ClinVar ID
nssv18791632	deletion	Multiple	Multiple	not provided	Pathogenic	ClinVar	RCV003105530.2, VCV002423836.2

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Inner Start	Inner Stop
nssv18791632	Remapped	Perfect	NC_000006.12:g.(?_ 65384366)_(6570722 5_?)del	GRCh38.p12	First Pass	NC_000006.12	Chr6	65,384,366	65,707,225
nssv18791632	Submitted genomic		NC_000006.11:g.(?_ 66094259)_(6641711 8_?)del	GRCh37 (hg19)		NC_000006.11	Chr6	66,094,259	66,417,118

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
nssv18791632	GRCh37: NC_000006.11:g.(?_66094259)_(66417118_?)del	deletion	germline	not provided	Pathogenic	ClinVar	RCV003105530.2, VCV002423836.2

No genotype data were submitted for this variant

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