A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv521357



Internal ID15448650
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:11166836..11175373hg38UCSC Ensembl
Innerchr5:11166948..11175485hg19UCSC Ensembl
Innerchr5:11219948..11228485hg18UCSC Ensembl
Innerchr5:11219948..11228485hg17UCSC Ensembl
Cytoband5p15.2
Allele length
AssemblyAllele length
hg388538
hg198538
hg188538
hg178538
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv694436
Samples
Known GenesCTNND2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv521357
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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