A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14105222



Internal ID21278812
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:58337555..58553531hg38UCSC Ensembl
Innerchr2:58564690..58780666hg19UCSC Ensembl
Cytoband2p16.1
Allele length
AssemblyAllele length
hg38215977
hg19215977
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3117976
Supporting Variants
Samplessample274
Known GenesLINC01122
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14105222
Frequency
Sample Size467
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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