A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14088266



Internal ID21286744
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:39480338..39528445hg38UCSC Ensembl
Innerchr8:39337857..39385964hg19UCSC Ensembl
Cytoband8p11.22
Allele length
AssemblyAllele length
hg3848108
hg1948108
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3116846
Supporting Variants
Samplessample393
Known GenesADAM3A
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14088266
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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