A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv520193



Internal ID15447486
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:99275688..99276761hg38UCSC Ensembl
Innerchr9:102037970..102039043hg19UCSC Ensembl
Innerchr9:101077791..101078864hg18UCSC Ensembl
Innerchr9:99117525..99118598hg17UCSC Ensembl
Cytoband9q22.33
Allele length
AssemblyAllele length
hg381074
hg191074
hg181074
hg171074
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv661590, nssv681753
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv520193
Frequency
Sample Size2026
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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