A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv522035



Internal ID15449328
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:21885368..21897262hg38UCSC Ensembl
Innerchr13:22459507..22471401hg19UCSC Ensembl
Innerchr13:21357507..21369401hg18UCSC Ensembl
Innerchr13:21357507..21369401hg17UCSC Ensembl
Cytoband13q12.11
Allele length
AssemblyAllele length
hg3811895
hg1911895
hg1811895
hg1711895
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv694805
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv522035
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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