A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14087184



Internal ID21269188
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:42392294..42393582hg38UCSC Ensembl
Innerchr8:42249812..42251100hg19UCSC Ensembl
Cytoband8p11.21
Allele length
AssemblyAllele length
hg381289
hg191289
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3117226
Supporting Variants
Samplessample136
Known GenesVDAC3
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14087184
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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