A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14106910



Internal ID21287091
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:156339753..156344979hg38UCSC Ensembl
Innerchr2:157196265..157201491hg19UCSC Ensembl
Cytoband2q24.1
Allele length
AssemblyAllele length
hg385227
hg195227
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3114624
Supporting Variants
Samplessample397
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14106910
Frequency
Sample Size467
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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