A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14109323



Internal ID21281230
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:79525454..79534818hg38UCSC Ensembl
Innerchr5:78821277..78830641hg19UCSC Ensembl
Cytoband5q14.1
Allele length
AssemblyAllele length
hg389365
hg199365
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3116095
Supporting Variants
Samplessample309
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14109323
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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