A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv833078



Internal ID16127034
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:100627840..100649196hg38UCSC Ensembl
Innerchr14:101094177..101115533hg19UCSC Ensembl
Innerchr14:100163930..100185286hg18UCSC Ensembl
Cytoband14q32.2
Allele length
AssemblyAllele length
hg3821357
hg1921357
hg1821357
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv565785
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)nssv833078
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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