A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14096648



Internal ID21288949
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:68569726..68748292hg38UCSC Ensembl
Innerchr4:69435444..69614010hg19UCSC Ensembl
Cytoband4q13.2
Allele length
AssemblyAllele length
hg38178567
hg19178567
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3112176
Supporting Variants
Samplessample424
Known GenesUGT2B15
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14096648
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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