A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv528298



Internal ID15455591
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:75902744..75936691hg38UCSC Ensembl
Innerchr2:76129870..76163817hg19UCSC Ensembl
Innerchr2:75983378..76017325hg18UCSC Ensembl
Innerchr2:76041525..76075472hg17UCSC Ensembl
Cytoband2p12
Allele length
AssemblyAllele length
hg3833948
hg1933948
hg1833948
hg1733948
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv704873
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv528298
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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