A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv930901



Internal ID16224857
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:208649191..208794498hg38UCSC Ensembl
Innerchr2:209513915..209659222hg19UCSC Ensembl
Innerchr2:209222160..209367467hg18UCSC Ensembl
Cytoband2q34
Allele length
AssemblyAllele length
hg38145308
hg19145308
hg18145308
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv584303
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv930901
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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