A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv700233



Internal ID15436885
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:9773386..9814639hg38UCSC Ensembl
Innerchr2:9913515..9954768hg19UCSC Ensembl
Innerchr2:9830966..9872219hg18UCSC Ensembl
Innerchr2:9864113..9905366hg17UCSC Ensembl
Cytoband2p25.1
Allele length
AssemblyAllele length
hg3841254
hg1941254
hg1841254
hg1741254
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv524327
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv700233
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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