A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv526502



Internal ID15453795
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:34513754..34904204hg38UCSC Ensembl
Innerchr13:35087891..35478341hg19UCSC Ensembl
Innerchr13:33985891..34376341hg18UCSC Ensembl
Innerchr13:33985891..34376341hg17UCSC Ensembl
Cytoband13q13.2
Allele length
AssemblyAllele length
hg38390451
hg19390451
hg18390451
hg17390451
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv702812
Samples
Known GenesLINC00457
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv526502
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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