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dbVar

Database of genomic structural variation

nsv6636481

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:543,250

Description:GRCh37/hg19 1p36.12-36.11(chr1:23680995-24224241)x3 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: 1941 SVs from 81 studies. See in: genome view

Remapped(Score: Good):23,354,502-23,897,751

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Inner Start	Inner Stop
nsv6636481	Remapped	Good	GRCh38.p12	Primary Assembly	First Pass	NC_000001.11	Chr1	23,354,502	23,897,751
nsv6636481	Submitted genomic		GRCh37 (hg19)	Primary Assembly		NC_000001.10	Chr1	23,680,995	24,224,241

Variant Call Information

Variant Call ID	Type	Method	Analysis	Subject Phenotype	Clinical Interpretation	Source of Interpretation	ClinVar ID	Copy number
nssv18330221	copy number gain	Multiple	Multiple	not provided	Uncertain significance	ClinVar	RCV002473953.1, VCV001808636.1	3

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Inner Start	Inner Stop
nssv18330221	Remapped	Good	NC_000001.11:g.(?_ 23354502)_(2389775 1_?)dup	GRCh38.p12	First Pass	NC_000001.11	Chr1	23,354,502	23,897,751
nssv18330221	Submitted genomic		NC_000001.10:g.(?_ 23680995)_(2422424 1_?)dup	GRCh37 (hg19)		NC_000001.10	Chr1	23,680,995	24,224,241

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
nssv18330221	GRCh37: NC_000001.10:g.(?_23680995)_(24224241_?)dup	copy number gain	unknown	not provided	Uncertain significance	ClinVar	RCV002473953.1, VCV001808636.1	3

No genotype data were submitted for this variant

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