A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3112128



Internal ID21295394
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:45349212..45362753hg38UCSC Ensembl
Innerchr13:45923347..45936888hg19UCSC Ensembl
Cytoband13q14.13
Allele length
AssemblyAllele length
hg3813542
hg1913542
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14092971
Samplessample403
Known GenesTPT1-AS1
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3112128
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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