A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv700929



Internal ID15437581
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:23826583..23890484hg38UCSC Ensembl
Innerchr2:24049453..24113354hg19UCSC Ensembl
Innerchr2:23902957..23966858hg18UCSC Ensembl
Innerchr2:23961104..24025005hg17UCSC Ensembl
Cytoband2p23.3
Allele length
AssemblyAllele length
hg3863902
hg1963902
hg1863902
hg1763902
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv524917
Supporting Variants
Samples
Known GenesATAD2B
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv700929
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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