A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv832735



Internal ID16126691
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:97337404..97337965hg38UCSC Ensembl
Innerchr14:97803741..97804302hg19UCSC Ensembl
Innerchr14:96873494..96874055hg18UCSC Ensembl
Cytoband14q32.2
Allele length
AssemblyAllele length
hg38562
hg19562
hg18562
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv565656
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)nssv832735
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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