A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv565168



Internal ID16352577
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:73559754..73580153hg38UCSC Ensembl
Innerchr14:74026458..74046857hg19UCSC Ensembl
Innerchr14:73096211..73116610hg18UCSC Ensembl
Cytoband14q24.3
Allele length
AssemblyAllele length
hg3820400
hg1920400
hg1820400
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3774n54
Supporting Variantsnssv829492
Samples
Known GenesACOT2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv565168
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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