A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14086071



Internal ID21274620
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:91642631..91648756hg38UCSC Ensembl
Innerchr8:92654859..92660984hg19UCSC Ensembl
Cytoband8q21.3
Allele length
AssemblyAllele length
hg386126
hg196126
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3116237
Supporting Variants
Samplessample209
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14086071
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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