A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv569594



Internal ID16357003
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:58044020..58055062hg38UCSC Ensembl
Innerchr15:58336218..58347260hg19UCSC Ensembl
Innerchr15:56123510..56134552hg18UCSC Ensembl
Cytoband15q21.3
Allele length
AssemblyAllele length
hg3811043
hg1911043
hg1811043
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv843573
Samples
Known GenesALDH1A2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv569594
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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