A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3579016



Internal ID18877297
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:23755930..23857418hg38UCSC Ensembl
Innerchr2:23978800..24080288hg19UCSC Ensembl
Innerchr2:23832304..23933792hg18UCSC Ensembl
Cytoband2p23.3
Allele length
AssemblyAllele length
hg38101489
hg19101489
hg18101489
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1014412
Supporting Variants
Samples
Known GenesATAD2B
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3579016
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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