A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv569593



Internal ID16010316
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:57909500..58016452hg38UCSC Ensembl
Innerchr15:58201698..58308650hg19UCSC Ensembl
Innerchr15:55988990..56095942hg18UCSC Ensembl
Cytoband15q21.3
Allele length
AssemblyAllele length
hg38106953
hg19106953
hg18106953
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv843572
Samples
Known GenesALDH1A2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv569593
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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