A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14102515



Internal ID21290607
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:44847003..44873259hg38UCSC Ensembl
Innerchr2:45074142..45100398hg19UCSC Ensembl
Cytoband2p21
Allele length
AssemblyAllele length
hg3826257
hg1926257
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3116354
Supporting Variants
Samplessample61
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14102515
Frequency
Sample Size467
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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