Warning: The NCBI web site requires JavaScript to function. more...

dbVar

Database of genomic structural variation

nsv3898580

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:51,686

Description:GRCh37/hg19 19p13.3(chr19:460883-512568)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: 863 SVs from 68 studies. See in: genome view

Remapped(Score: Perfect):460,883-512,568

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Inner Start	Inner Stop
nsv3898580	Remapped	Perfect	GRCh38.p12	Primary Assembly	First Pass	NC_000019.10	Chr19	460,883	512,568
nsv3898580	Submitted genomic		GRCh37 (hg19)	Primary Assembly		NC_000019.9	Chr19	460,883	512,568

Variant Call Information

Variant Call ID	Type	Method	Analysis	Subject Phenotype	Clinical Interpretation	Source of Interpretation	ClinVar ID	Copy number
nssv15173867	copy number gain	Multiple	Multiple	not provided	Benign	ClinVar	RCV000752451.2, VCV000615815.2	3

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Inner Start	Inner Stop
nssv15173867	Remapped	Perfect	NC_000019.10:g.(?_ 460883)_(512568_?) dup	GRCh38.p12	First Pass	NC_000019.10	Chr19	460,883	512,568
nssv15173867	Submitted genomic		NC_000019.9:g.(?_4 60883)_(512568_?)d up	GRCh37 (hg19)		NC_000019.9	Chr19	460,883	512,568

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
nssv15173867	GRCh37: NC_000019.9:g.(?_460883)_(512568_?)dup	copy number gain	unknown	not provided	Benign	ClinVar	RCV000752451.2, VCV000615815.2	3

No genotype data were submitted for this variant

You are here: NCBI