A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv934903



Internal ID16228859
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:241931649..242078572hg38UCSC Ensembl
Innerchr2:242873800..243020723hg19UCSC Ensembl
Innerchr2:242522473..242669396hg18UCSC Ensembl
Cytoband2q37.3
Allele length
AssemblyAllele length
hg38146924
hg19146924
hg18146924
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv585046
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)nssv934903
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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