A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv829372



Internal ID15776642
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:73534773..73559754hg38UCSC Ensembl
Innerchr14:74001477..74026458hg19UCSC Ensembl
Innerchr14:73071230..73096211hg18UCSC Ensembl
Cytoband14q24.3
Allele length
AssemblyAllele length
hg3824982
hg1924982
hg1824982
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv565148
Supporting Variants
Samples
Known GenesACOT1, HEATR4
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv829372
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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