A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14087099



Internal ID21267644
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:39375671..39530975hg38UCSC Ensembl
Innerchr8:39233190..39388494hg19UCSC Ensembl
Cytoband8p11.22
Allele length
AssemblyAllele length
hg38155305
hg19155305
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3116328
Supporting Variants
Samplessample115
Known GenesADAM3A, ADAM5
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14087099
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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