A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv526566



Internal ID15453859
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:48115341..48120112hg38UCSC Ensembl
Innerchr14:48584544..48589315hg19UCSC Ensembl
Innerchr14:47654294..47659065hg18UCSC Ensembl
Innerchr14:47654294..47659065hg17UCSC Ensembl
Cytoband14q21.3
Allele length
AssemblyAllele length
hg384772
hg194772
hg184772
hg174772
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv702882
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv526566
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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