A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv834882



Internal ID16128838
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:105474277..105475085hg38UCSC Ensembl
Innerchr14:105940614..105941422hg19UCSC Ensembl
Innerchr14:105011659..105012467hg18UCSC Ensembl
Cytoband14q32.33
Allele length
AssemblyAllele length
hg38809
hg19809
hg18809
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv566239
Supporting Variants
Samples
Known GenesCRIP2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv834882
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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