A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv527063



Internal ID15454356
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:38396068..38396505hg38UCSC Ensembl
Innerchr9:38396065..38396502hg19UCSC Ensembl
Innerchr9:38386065..38386502hg18UCSC Ensembl
Innerchr9:38386065..38386502hg17UCSC Ensembl
Cytoband9p13.1
Allele length
AssemblyAllele length
hg38438
hg19438
hg18438
hg17438
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv703442
Samples
Known GenesALDH1B1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv527063
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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