A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv653855



Internal ID15390507
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:49961727..49971221hg38UCSC Ensembl
Innerchr13:50535863..50545357hg19UCSC Ensembl
Innerchr13:49433864..49443358hg18UCSC Ensembl
Innerchr13:49433864..49443358hg17UCSC Ensembl
Cytoband13q14.2
Allele length
AssemblyAllele length
hg389495
hg199495
hg189495
hg179495
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517142
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv653855
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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