A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv565138



Internal ID16005861
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:73534075..73544816hg38UCSC Ensembl
Innerchr14:74000779..74011520hg19UCSC Ensembl
Innerchr14:73070532..73081273hg18UCSC Ensembl
Cytoband14q24.3
Allele length
AssemblyAllele length
hg3810742
hg1910742
hg1810742
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3767n54
Supporting Variantsnssv829342
Samples
Known GenesACOT1, HEATR4
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv565138
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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