A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv925614



Internal ID15872884
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:176070797..176134284hg38UCSC Ensembl
Innerchr2:176935525..176999012hg19UCSC Ensembl
Innerchr2:176643771..176707258hg18UCSC Ensembl
Cytoband2q31.1
Allele length
AssemblyAllele length
hg3863488
hg1963488
hg1863488
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv583672
Supporting Variants
Samples
Known GenesEVX2, HOXD10, HOXD11, HOXD12, HOXD13, HOXD8, HOXD9
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv925614
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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