A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv521608



Internal ID15448901
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:112372077..112379694hg38UCSC Ensembl
Innerchr9:115134357..115141974hg19UCSC Ensembl
Innerchr9:114174178..114181795hg18UCSC Ensembl
Innerchr9:112213912..112221529hg17UCSC Ensembl
Cytoband9q32
Allele length
AssemblyAllele length
hg387618
hg197618
hg187618
hg177618
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv698225
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv521608
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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