A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv831938



Internal ID16125894
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:85011263..85032821hg38UCSC Ensembl
Innerchr14:85477607..85499165hg19UCSC Ensembl
Innerchr14:84547360..84568918hg18UCSC Ensembl
Cytoband14q31.3
Allele length
AssemblyAllele length
hg3821559
hg1921559
hg1821559
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv565424
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)nssv831938
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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