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

dbVar

Database of genomic structural variation

nsv7098718

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:2,564,829

Description:
NC_000019.9:g.(?_1206913)_(3771740_?)dup 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: 13000 SVs from 107 studies. See in: genome view

Remapped(Score: Perfect):1,206,914-3,771,742

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Inner Start	Inner Stop
nsv7098718	Remapped	Perfect	GRCh38.p12	Primary Assembly	First Pass	NC_000019.10	Chr19	1,206,914	3,771,742
nsv7098718	Submitted genomic		GRCh37 (hg19)	Primary Assembly		NC_000019.9	Chr19	1,206,913	3,771,740

Variant Call Information

Variant Call ID	Type	Method	Analysis	Subject Phenotype	Clinical Interpretation	Source of Interpretation	ClinVar ID
nssv18792637	duplication	Multiple	Multiple	not provided	Uncertain significance	ClinVar	RCV003154903.1, VCV002445494.1

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Inner Start	Inner Stop
nssv18792637	Remapped	Perfect	NC_000019.10:g.(?_ 1206914)_(3771742_ ?)dup	GRCh38.p12	First Pass	NC_000019.10	Chr19	1,206,914	3,771,742
nssv18792637	Submitted genomic		NC_000019.9:g.(?_1 206913)_(3771740_? )dup	GRCh37 (hg19)		NC_000019.9	Chr19	1,206,913	3,771,740

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
nssv18792637	GRCh37: NC_000019.9:g.(?_1206913)_(3771740_?)dup	duplication	germline	not provided	Uncertain significance	ClinVar	RCV003154903.1, VCV002445494.1

No genotype data were submitted for this variant

You are here: NCBI