A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv932913



Internal ID16226869
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:226286575..226305908hg38UCSC Ensembl
Innerchr2:227151291..227170624hg19UCSC Ensembl
Innerchr2:226859535..226878868hg18UCSC Ensembl
Cytoband2q36.3
Allele length
AssemblyAllele length
hg3819334
hg1919334
hg1819334
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv584562
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)nssv932913
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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