A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv831950



Internal ID16125906
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:85816380..85845829hg38UCSC Ensembl
Innerchr14:86282724..86312173hg19UCSC Ensembl
Innerchr14:85352477..85381926hg18UCSC Ensembl
Cytoband14q31.3
Allele length
AssemblyAllele length
hg3829450
hg1929450
hg1829450
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv565434
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)nssv831950
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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