A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv827612



Internal ID16121568
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:44612384..44739573hg38UCSC Ensembl
Innerchr14:45081587..45208776hg19UCSC Ensembl
Innerchr14:44151337..44278526hg18UCSC Ensembl
Cytoband14q21.2
Allele length
AssemblyAllele length
hg38127190
hg19127190
hg18127190
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv564697
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)nssv827612
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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