A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14092971



Internal ID21287612
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 StatusS
Merged Variantsnsv3112128
Supporting Variants
Samplessample403
Known GenesTPT1-AS1
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14092971
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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