A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv518610



Internal ID15445903
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:28901735..28912107hg38UCSC Ensembl
Innerchr13:29475872..29486244hg19UCSC Ensembl
Innerchr13:28373872..28384244hg18UCSC Ensembl
Innerchr13:28373872..28384244hg17UCSC Ensembl
Cytoband13q12.3
Allele length
AssemblyAllele length
hg3810373
hg1910373
hg1810373
hg1710373
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv694253
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv518610
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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