A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv565141



Internal ID16005864
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:73534434..73543861hg38UCSC Ensembl
Innerchr14:74001138..74010565hg19UCSC Ensembl
Innerchr14:73070891..73080318hg18UCSC Ensembl
Cytoband14q24.3
Allele length
AssemblyAllele length
hg389428
hg199428
hg189428
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3767n54
Supporting Variantsnssv829355, nssv829356
Samples
Known GenesACOT1, HEATR4
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv565141
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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