A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14084612



Internal ID21274701
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:155049065..155054408hg38UCSC Ensembl
Innerchr7:154840775..154846118hg19UCSC Ensembl
Cytoband7q36.2
Allele length
AssemblyAllele length
hg385344
hg195344
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3115323
Supporting Variants
Samplessample210
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14084612
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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