A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv521697



Internal ID15102304
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:17211540..17225224hg38UCSC Ensembl
Innerchr5:17211649..17225333hg19UCSC Ensembl
Innerchr5:17264649..17278333hg18UCSC Ensembl
Innerchr5:17264649..17278333hg17UCSC Ensembl
Cytoband5p15.1
Allele length
AssemblyAllele length
hg3813685
hg1913685
hg1813685
hg1713685
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv698318
Samples
Known GenesBASP1, LOC285696
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv521697
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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