A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1148631



Internal ID15508422
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:104969312..105223755hg38UCSC Ensembl
Innerchr14:105435649..105690092hg19UCSC Ensembl
Innerchr14:104506694..104761137hg18UCSC Ensembl
Cytoband14q32.33
Allele length
AssemblyAllele length
hg38254444
hg19254444
hg18254444
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv566150
Supporting Variants
Samples1780862444_A
Known GenesAHNAK2, BRF1, C14orf79, CDCA4, GPR132, JAG2, MIR6765, NUDT14
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1148631
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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