A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv528812



Internal ID15456105
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:94489813..94490580hg38UCSC Ensembl
Innerchr13:95142067..95142834hg19UCSC Ensembl
Innerchr13:93940068..93940835hg18UCSC Ensembl
Innerchr13:93940068..93940835hg17UCSC Ensembl
Cytoband13q32.1
Allele length
AssemblyAllele length
hg38768
hg19768
hg18768
hg17768
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv705486
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv528812
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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