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

dbVar

Database of genomic structural variation

nsv8710

Organism: Homo sapiens

Study:nstd4 (Perry et al. 2008)
Variant Type:copy number variation
Method Type:Oligo aCGH
Submitted on:NCBI35 (hg17)

Variant Calls:1
Validation:Not tested
Clinical Assertions: No
Region Size:243,319

Publication(s):Perry et al. 2008

Links to Other Resources

Overlapping Genes

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: 248 SVs from 31 studies. See in: genome view

Remapped(Score: Perfect):80,857,435-81,100,753

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Outer Start	Outer Stop
nsv8710	Remapped	Perfect	GRCh38.p12	Primary Assembly	First Pass	NC_000010.11	Chr10	80,857,435	81,100,753
nsv8710	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000010.10	Chr10	82,617,191	82,860,509
nsv8710	Submitted genomic		NCBI35 (hg17)	Primary Assembly		NC_000010.8	Chr10	82,607,171	82,850,489

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Other Calls in this Sample and Study
nssv20167	copy number loss	NA11830	Oligo aCGH	Probe signal intensity	568

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Outer Start	Inner Start	Inner Stop	Outer Stop
nssv20167	Remapped	Perfect	NC_000010.11:g.(80 857435_80959028)_( 81015337_81100753) del	GRCh38.p12	First Pass	NC_000010.11	Chr10	80,857,435	80,959,028	81,015,337	81,100,753
nssv20167	Remapped	Perfect	NC_000010.10:g.(82 617191_82718784)_( 82775093_82860509) del	GRCh37.p13	First Pass	NC_000010.10	Chr10	82,617,191	82,718,784	82,775,093	82,860,509
nssv20167	Submitted genomic		NC_000010.8:g.(826 07171_82708764)_(8 2765073_82850489)d el	NCBI35 (hg17)		NC_000010.8	Chr10	82,607,171	82,708,764	82,765,073	82,850,489

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