A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv934890



Internal ID16228846
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:241931649..242065217hg38UCSC Ensembl
Innerchr2:242873800..243007368hg19UCSC Ensembl
Innerchr2:242522473..242656041hg18UCSC Ensembl
Cytoband2q37.3
Allele length
AssemblyAllele length
hg38133569
hg19133569
hg18133569
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv585044
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)nssv934890
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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