A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv526377



Internal ID15106984
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:23003729..23007109hg38UCSC Ensembl
Innerchr8:22861242..22864622hg19UCSC Ensembl
Innerchr8:22917187..22920567hg18UCSC Ensembl
Innerchr8:22917187..22920567hg17UCSC Ensembl
Cytoband8p21.3
Allele length
AssemblyAllele length
hg383381
hg193381
hg183381
hg173381
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv702673
Samples
Known GenesRHOBTB2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv526377
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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