A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv565162



Internal ID16352571
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:73549270..73582351hg38UCSC Ensembl
Innerchr14:74015974..74049055hg19UCSC Ensembl
Innerchr14:73085727..73118808hg18UCSC Ensembl
Cytoband14q24.3
Allele length
AssemblyAllele length
hg3833082
hg1933082
hg1833082
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv829482
Samples
Known GenesACOT2, HEATR4
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv565162
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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