A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14105797



Internal ID21276144
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:68103631..68126461hg38UCSC Ensembl
Innerchr2:68330763..68353593hg19UCSC Ensembl
Cytoband2p14
Allele length
AssemblyAllele length
hg3822831
hg1922831
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3110388
Supporting Variants
Samplessample232
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14105797
Frequency
Sample Size467
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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