A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv524566



Internal ID15105173
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:22094715..22131002hg38UCSC Ensembl
Innerchr8:21952226..21988515hg19UCSC Ensembl
Innerchr8:22008172..22044460hg18UCSC Ensembl
Innerchr8:22008172..22044460hg17UCSC Ensembl
Cytoband8p21.3
Allele length
AssemblyAllele length
hg3836288
hg1936290
hg1836289
hg1736289
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv450n21
Supporting Variantsnssv700521
Samples
Known GenesFAM160B2, HR, NUDT18
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv524566
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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