A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv523017



Internal ID15450310
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:122239706..122245614hg38UCSC Ensembl
Innerchr9:125001985..125007893hg19UCSC Ensembl
Innerchr9:124041806..124047714hg18UCSC Ensembl
Innerchr9:122081539..122087447hg17UCSC Ensembl
Cytoband9q33.2
Allele length
AssemblyAllele length
hg385909
hg195909
hg185909
hg175909
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv698693
Samples
Known GenesRBM18
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv523017
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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