A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14108792



Internal ID21271232
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:170487376..170701955hg38UCSC Ensembl
Innerchr5:169914380..170128959hg19UCSC Ensembl
Cytoband5q35.1
Allele length
AssemblyAllele length
hg38214580
hg19214580
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3111391
Supporting Variants
Samplessample160
Known GenesKCNIP1
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14108792
Frequency
Sample Size467
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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