A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv527646



Internal ID15454939
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:38636466..38646998hg38UCSC Ensembl
Innerchr9:38636463..38646995hg19UCSC Ensembl
Innerchr9:38626463..38636995hg18UCSC Ensembl
Innerchr9:38626463..38636995hg17UCSC Ensembl
Cytoband9p13.1
Allele length
AssemblyAllele length
hg3810533
hg1910533
hg1810533
hg1710533
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv704117
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv527646
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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