A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv522436



Internal ID15103043
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:23003729..23014544hg38UCSC Ensembl
Innerchr8:22861242..22872057hg19UCSC Ensembl
Innerchr8:22917187..22928002hg18UCSC Ensembl
Innerchr8:22917187..22928002hg17UCSC Ensembl
Cytoband8p21.3
Allele length
AssemblyAllele length
hg3810816
hg1910816
hg1810816
hg1710816
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv705794
Samples
Known GenesRHOBTB2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv522436
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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