A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv834811



Internal ID15782081
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:105465248..105499970hg38UCSC Ensembl
Innerchr14:105931585..105966307hg19UCSC Ensembl
Innerchr14:105002630..105037352hg18UCSC Ensembl
Cytoband14q32.33
Allele length
AssemblyAllele length
hg3834723
hg1934723
hg1834723
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv566211
Supporting Variants
Samples
Known GenesC14orf80, CRIP1, CRIP2, MTA1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv834811
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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