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dbVar

Database of genomic structural variation

nsv6637942

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:56,284

Description:GRCh37/hg19 13q14.11(chr13:43354951-43411234)x1 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: 254 SVs from 44 studies. See in: genome view

Remapped(Score: Perfect):42,780,815-42,837,098

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Inner Start	Inner Stop
nsv6637942	Remapped	Perfect	GRCh38.p12	Primary Assembly	First Pass	NC_000013.11	Chr13	42,780,815	42,837,098
nsv6637942	Submitted genomic		GRCh37 (hg19)	Primary Assembly		NC_000013.10	Chr13	43,354,951	43,411,234

Variant Call Information

Variant Call ID	Type	Method	Analysis	Subject Phenotype	Clinical Interpretation	Source of Interpretation	ClinVar ID	Copy number
nssv18328910	copy number loss	Multiple	Multiple	not provided	Uncertain significance	ClinVar	RCV002474896.1, VCV001809051.1	1

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Inner Start	Inner Stop
nssv18328910	Remapped	Perfect	NC_000013.11:g.(?_ 42780815)_(4283709 8_?)del	GRCh38.p12	First Pass	NC_000013.11	Chr13	42,780,815	42,837,098
nssv18328910	Submitted genomic		NC_000013.10:g.(?_ 43354951)_(4341123 4_?)del	GRCh37 (hg19)		NC_000013.10	Chr13	43,354,951	43,411,234

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
nssv18328910	GRCh37: NC_000013.10:g.(?_43354951)_(43411234_?)del	copy number loss	unknown	not provided	Uncertain significance	ClinVar	RCV002474896.1, VCV001809051.1	1

No genotype data were submitted for this variant

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