A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv826838



Internal ID16120794
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:41141404..41198356hg38UCSC Ensembl
Innerchr14:41610607..41667559hg19UCSC Ensembl
Innerchr14:40680357..40737309hg18UCSC Ensembl
Cytoband14q21.1
Allele length
AssemblyAllele length
hg3856953
hg1956953
hg1856953
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv564495
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)nssv826838
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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