A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14108794



Internal ID21271220
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:170705417..170794879hg38UCSC Ensembl
Innerchr5:170132421..170221883hg19UCSC Ensembl
Cytoband5q35.1
Allele length
AssemblyAllele length
hg3889463
hg1989463
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3115254
Supporting Variants
Samplessample160
Known GenesGABRP, KCNIP1
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14108794
Frequency
Sample Size467
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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