A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv523829



Internal ID15451122
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:108007714..108019216hg38UCSC Ensembl
Innerchr13:108660062..108671564hg19UCSC Ensembl
Innerchr13:107458063..107469565hg18UCSC Ensembl
Innerchr13:107458063..107469565hg17UCSC Ensembl
Cytoband13q33.3
Allele length
AssemblyAllele length
hg3811503
hg1911503
hg1811503
hg1711503
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv699660
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv523829
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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