A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv828623



Internal ID15775893
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:66962955..66986676hg38UCSC Ensembl
Innerchr14:67429672..67453393hg19UCSC Ensembl
Innerchr14:66499425..66523146hg18UCSC Ensembl
Cytoband14q23.3
Allele length
AssemblyAllele length
hg3823722
hg1923722
hg1823722
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv564958
Supporting Variants
Samples
Known GenesGPHN
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv828623
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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