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dbVar

Database of genomic structural variation

nsv5673947

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:1,136

Description:NC_000008.10:g.(?_143998465)_(143999600_?)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: 101 SVs from 25 studies. See in: genome view

Remapped(Score: Perfect):142,917,049-142,918,184

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Inner Start	Inner Stop
nsv5673947	Remapped	Perfect	GRCh38.p12	Primary Assembly	First Pass	NC_000008.11	Chr8	142,917,049	142,918,184
nsv5673947	Submitted genomic		GRCh37 (hg19)	Primary Assembly		NC_000008.10	Chr8	143,998,465	143,999,600

Variant Call Information

Variant Call ID	Type	Method	Analysis	Subject Phenotype	Clinical Interpretation	Source of Interpretation	ClinVar ID
nssv17171639	deletion	Multiple	Multiple	not provided	Pathogenic	ClinVar	RCV001387703.3, VCV001074429.3

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Inner Start	Inner Stop
nssv17171639	Remapped	Perfect	NC_000008.11:g.(?_ 142917049)_(142918 184_?)del	GRCh38.p12	First Pass	NC_000008.11	Chr8	142,917,049	142,918,184
nssv17171639	Submitted genomic		NC_000008.10:g.(?_ 143998465)_(143999 600_?)del	GRCh37 (hg19)		NC_000008.10	Chr8	143,998,465	143,999,600

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
nssv17171639	GRCh37: NC_000008.10:g.(?_143998465)_(143999600_?)del	deletion	germline	not provided	Pathogenic	ClinVar	RCV001387703.3, VCV001074429.3

No genotype data were submitted for this variant

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