A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv524119



Internal ID15104726
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:101006159..101075321hg38UCSC Ensembl
Innerchr8:102018387..102087549hg19UCSC Ensembl
Innerchr8:102087563..102156725hg18UCSC Ensembl
Innerchr8:102087563..102156725hg17UCSC Ensembl
Cytoband8q22.3
Allele length
AssemblyAllele length
hg3869163
hg1969163
hg1869163
hg1769163
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv699997
Samples
Known GenesFLJ42969
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv524119
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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