A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14108856



Internal ID21272133
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:172605321..172609265hg38UCSC Ensembl
Innerchr5:172032324..172036268hg19UCSC Ensembl
Cytoband5q35.1
Allele length
AssemblyAllele length
hg383945
hg193945
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3114844
Supporting Variants
Samplessample173
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14108856
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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