A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv520028



Internal ID15447321
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:51740106..51759201hg38UCSC Ensembl
Innerchr2:51967244..51986339hg19UCSC Ensembl
Innerchr2:51820748..51839843hg18UCSC Ensembl
Innerchr2:51878895..51897990hg17UCSC Ensembl
Cytoband2p16.3
Allele length
AssemblyAllele length
hg3819096
hg1919096
hg1819096
hg1719096
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv660149, nssv693012
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv520028
Frequency
Sample Size2026
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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