A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv526357



Internal ID15106964
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:90734186..90746498hg38UCSC Ensembl
Innerchr13:91386440..91398752hg19UCSC Ensembl
Innerchr13:90184441..90196753hg18UCSC Ensembl
Innerchr13:90184441..90196753hg17UCSC Ensembl
Cytoband13q31.3
Allele length
AssemblyAllele length
hg3812313
hg1912313
hg1812313
hg1712313
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv116n21
Supporting Variantsnssv702650
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv526357
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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