A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv569596



Internal ID16010319
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:58063600..58116564hg38UCSC Ensembl
Innerchr15:58355798..58408763hg19UCSC Ensembl
Innerchr15:56143090..56196055hg18UCSC Ensembl
Cytoband15q21.3
Allele length
AssemblyAllele length
hg3852965
hg1952966
hg1852966
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv843575
Samples
Known GenesALDH1A2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv569596
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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