A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv522634



Internal ID15449927
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:80281941..80284999hg38UCSC Ensembl
Innerchr5:79577760..79580818hg19UCSC Ensembl
Innerchr5:79613516..79616574hg18UCSC Ensembl
Innerchr5:79613516..79616574hg17UCSC Ensembl
Cytoband5q14.1
Allele length
AssemblyAllele length
hg383059
hg193059
hg183059
hg173059
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv706032
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv522634
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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