A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv518191



Internal ID15445484
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:97662078..97663027hg38UCSC Ensembl
Innerchr13:98314332..98315281hg19UCSC Ensembl
Innerchr13:97112333..97113282hg18UCSC Ensembl
Innerchr13:97112333..97113282hg17UCSC Ensembl
Cytoband13q32.2
Allele length
AssemblyAllele length
hg38950
hg19950
hg18950
hg17950
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv695614
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv518191
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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