A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv515653



Internal ID15443264
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:46190507..46193108hg38UCSC Ensembl
Innerchr2:46417646..46420247hg19UCSC Ensembl
Innerchr2:46271150..46273751hg18UCSC Ensembl
Innerchr2:46329297..46331898hg17UCSC Ensembl
Cytoband2p21
Allele length
AssemblyAllele length
hg382602
hg192602
hg182602
hg172602
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv664255, nssv681195
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv515653
Frequency
Sample Size2026
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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