A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv934901



Internal ID16228857
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:241931649..242075242hg38UCSC Ensembl
Innerchr2:242873800..243017393hg19UCSC Ensembl
Innerchr2:242522473..242666066hg18UCSC Ensembl
Cytoband2q37.3
Allele length
AssemblyAllele length
hg38143594
hg19143594
hg18143594
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv585045
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)nssv934901
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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