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

dbVar

Database of genomic structural variation

nsv4418031

Organism: Homo sapiens

Study:nstd174 (DGV Gold Standard)
Variant Type:copy number variation
Method Type:Multiple
Submitted on:GRCh37 (hg19)

Variant Calls:1
Validation:Not tested
Clinical Assertions: No
Region Size:236,828

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: 961 SVs from 73 studies. See in: genome view

Remapped(Score: Perfect):33,042,019-33,278,846

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Outer Start	Inner Start	Inner Stop	Outer Stop
nsv4418031	Remapped	Perfect	GRCh38.p12	Primary Assembly	First Pass	NC_000009.12	Chr9	33,042,019	33,086,300	33,254,684	33,278,846
nsv4418031	Submitted genomic		GRCh37 (hg19)	Primary Assembly		NC_000009.11	Chr9	33,042,017	33,086,298	33,254,682	33,278,844

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv15713202	copy number gain	Multiple	Multiple

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Outer Start	Inner Start	Inner Stop	Outer Stop
nssv15713202	Remapped	Perfect	NC_000009.12:g.(33 042019_33086300)_( 33254684_33278846) dup	GRCh38.p12	First Pass	NC_000009.12	Chr9	33,042,019	33,086,300	33,254,684	33,278,846
nssv15713202	Submitted genomic		NC_000009.11:g.(33 042017_33086298)_( 33254682_33278844) dup	GRCh37 (hg19)		NC_000009.11	Chr9	33,042,017	33,086,298	33,254,682	33,278,844

No validation data were submitted for this variant

No clinical assertion data were submitted for this variant

No genotype data were submitted for this variant

You are here: NCBI