A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14106897



Internal ID21286900
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:82301607..82324416hg38UCSC Ensembl
Innerchr2:82528731..82551540hg19UCSC Ensembl
Cytoband2p12
Allele length
AssemblyAllele length
hg3822810
hg1922810
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3113918
Supporting Variants
Samplessample395
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14106897
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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