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dbVar

Database of genomic structural variation

nsv7096519

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:9,104

Description:NC_000002.11:g.(?_62058213)_(62067316_?)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: 167 SVs from 34 studies. See in: genome view

Remapped(Score: Perfect):61,831,078-61,840,181

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Inner Start	Inner Stop
nsv7096519	Remapped	Perfect	GRCh38.p12	Primary Assembly	First Pass	NC_000002.12	Chr2	61,831,078	61,840,181
nsv7096519	Submitted genomic		GRCh37 (hg19)	Primary Assembly		NC_000002.11	Chr2	62,058,213	62,067,316

Variant Call Information

Variant Call ID	Type	Method	Analysis	Subject Phenotype	Clinical Interpretation	Source of Interpretation	ClinVar ID
nssv18791757	deletion	Multiple	Multiple	not provided	Likely pathogenic	ClinVar	RCV003105663.2, VCV002423968.2

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Inner Start	Inner Stop
nssv18791757	Remapped	Perfect	NC_000002.12:g.(?_ 61831078)_(6184018 1_?)del	GRCh38.p12	First Pass	NC_000002.12	Chr2	61,831,078	61,840,181
nssv18791757	Submitted genomic		NC_000002.11:g.(?_ 62058213)_(6206731 6_?)del	GRCh37 (hg19)		NC_000002.11	Chr2	62,058,213	62,067,316

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
nssv18791757	GRCh37: NC_000002.11:g.(?_62058213)_(62067316_?)del	deletion	germline	not provided	Likely pathogenic	ClinVar	RCV003105663.2, VCV002423968.2

No genotype data were submitted for this variant

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