A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv660835



Internal ID15397487
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:41012317..41017909hg38UCSC Ensembl
Innerchr2:41239457..41245049hg19UCSC Ensembl
Innerchr2:41092961..41098553hg18UCSC Ensembl
Innerchr2:41151108..41156700hg17UCSC Ensembl
Cytoband2p22.1
Allele length
AssemblyAllele length
hg385593
hg195593
hg185593
hg175593
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv515841
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv660835
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer