A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv614271



Internal ID16401680
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:38373833..38393212hg38UCSC Ensembl
Innerchr9:38373830..38393209hg19UCSC Ensembl
Innerchr9:38363830..38383209hg18UCSC Ensembl
Cytoband9p13.1
Allele length
AssemblyAllele length
hg3819380
hg1919380
hg1819380
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1134060
Samples
Known GenesALDH1B1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv614271
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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