A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv519867



Internal ID15447160
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:35593041..35862576hg38UCSC Ensembl
Innerchr2:35818107..36087642hg19UCSC Ensembl
Innerchr2:35671611..35941146hg18UCSC Ensembl
Innerchr2:35729758..35999293hg17UCSC Ensembl
Cytoband2p22.3
Allele length
AssemblyAllele length
hg38269536
hg19269536
hg18269536
hg17269536
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv686276, nssv699422, nssv694581, nssv676691, nssv698222, nssv659176, nssv704182
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv519867
Frequency
Sample Size2026
Observed Gain0
Observed Loss7
Observed Complex0
Frequencyn/a


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