A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv520321



Internal ID15100928
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:92893948..92905554hg38UCSC Ensembl
Innerchr8:93906176..93917782hg19UCSC Ensembl
Innerchr8:93975352..93986958hg18UCSC Ensembl
Innerchr8:93975352..93986958hg17UCSC Ensembl
Cytoband8q22.1
Allele length
AssemblyAllele length
hg3811607
hg1911607
hg1811607
hg1711607
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv697347
Samples
Known GenesTRIQK
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv520321
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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