A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv526145



Internal ID15453438
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:37745709..37836307hg38UCSC Ensembl
Innerchr11:37767259..37857857hg19UCSC Ensembl
Innerchr11:37723835..37814433hg18UCSC Ensembl
Innerchr11:37723835..37814433hg17UCSC Ensembl
Cytoband11p12
Allele length
AssemblyAllele length
hg3890599
hg1990599
hg1890599
hg1790599
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv702400
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv526145
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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