A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv526460



Internal ID15453753
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:112182341..112186966hg38UCSC Ensembl
Innerchr13:112836655..112841280hg19UCSC Ensembl
Innerchr13:111884656..111889281hg18UCSC Ensembl
Innerchr13:111884656..111889281hg17UCSC Ensembl
Cytoband13q34
Allele length
AssemblyAllele length
hg384626
hg194626
hg184626
hg174626
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv702763
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv526460
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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