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dbVar

Database of genomic structural variation

nsv3879141

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:953

Description:GRCh37/hg19 4p16.3(chr4:2263469-2264421)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: 324 SVs from 34 studies. See in: genome view

Remapped(Score: Perfect):2,261,742-2,262,694

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Inner Start	Inner Stop
nsv3879141	Remapped	Perfect	GRCh38.p12	Primary Assembly	First Pass	NC_000004.12	Chr4	2,261,742	2,262,694
nsv3879141	Submitted genomic		GRCh37 (hg19)	Primary Assembly		NC_000004.11	Chr4	2,263,469	2,264,421

Variant Call Information

Variant Call ID	Type	Method	Analysis	Subject Phenotype	Clinical Interpretation	Source of Interpretation	ClinVar ID	Copy number
nssv15164333	copy number gain	Multiple	Multiple	not provided	Benign	ClinVar	RCV000743233.2, VCV000606597.2	3

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Inner Start	Inner Stop
nssv15164333	Remapped	Perfect	NC_000004.12:g.(?_ 2261742)_(2262694_ ?)dup	GRCh38.p12	First Pass	NC_000004.12	Chr4	2,261,742	2,262,694
nssv15164333	Submitted genomic		NC_000004.11:g.(?_ 2263469)_(2264421_ ?)dup	GRCh37 (hg19)		NC_000004.11	Chr4	2,263,469	2,264,421

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
nssv15164333	GRCh37: NC_000004.11:g.(?_2263469)_(2264421_?)dup	copy number gain	unknown	not provided	Benign	ClinVar	RCV000743233.2, VCV000606597.2	3

No genotype data were submitted for this variant

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