A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14105872



Internal ID21277106
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:188156617..188202844hg38UCSC Ensembl
Innerchr2:189021344..189067571hg19UCSC Ensembl
Cytoband2q32.1
Allele length
AssemblyAllele length
hg3846228
hg1946228
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3110321
Supporting Variants
Samplessample245
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14105872
Frequency
Sample Size467
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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