A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv524038



Internal ID15451331
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:34765870..34848540hg38UCSC Ensembl
Innerchr2:34990937..35073607hg19UCSC Ensembl
Innerchr2:34844441..34927111hg18UCSC Ensembl
Innerchr2:34902588..34985258hg17UCSC Ensembl
Cytoband2p22.3
Allele length
AssemblyAllele length
hg3882671
hg1982671
hg1882671
hg1782671
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv699902
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv524038
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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