A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv824389



Internal ID15771659
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:24307195..24327607hg38UCSC Ensembl
Innerchr14:24776401..24796813hg19UCSC Ensembl
Innerchr14:23846241..23866653hg18UCSC Ensembl
Cytoband14q12
Allele length
AssemblyAllele length
hg3820413
hg1920413
hg1820413
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv564059
Supporting Variants
Samples
Known GenesADCY4, CIDEB, LTB4R, LTB4R2, NOP9
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv824389
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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