A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv565164



Internal ID16352573
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:73556034..73579080hg38UCSC Ensembl
Innerchr14:74022738..74045784hg19UCSC Ensembl
Innerchr14:73092491..73115537hg18UCSC Ensembl
Cytoband14q24.3
Allele length
AssemblyAllele length
hg3823047
hg1923047
hg1823047
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3774n54
Supporting Variantsnssv829484
Samples
Known GenesACOT2, HEATR4
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv565164
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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