A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv522371



Internal ID15449664
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:70838852..70856453hg38UCSC Ensembl
Innerchr13:71412984..71430585hg19UCSC Ensembl
Innerchr13:70310985..70328586hg18UCSC Ensembl
Innerchr13:70310985..70328586hg17UCSC Ensembl
Cytoband13q21.33
Allele length
AssemblyAllele length
hg3817602
hg1917602
hg1817602
hg1717602
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv112n21
Supporting Variantsnssv695151
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv522371
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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