A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv832121



Internal ID16126077
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:86349119..86355347hg38UCSC Ensembl
Innerchr14:86815463..86821691hg19UCSC Ensembl
Innerchr14:85885216..85891444hg18UCSC Ensembl
Cytoband14q31.3
Allele length
AssemblyAllele length
hg386229
hg196229
hg186229
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv565491
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)nssv832121
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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