A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14104692



Internal ID21270279
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:144515251..144518768hg38UCSC Ensembl
Innerchr2:145272818..145276335hg19UCSC Ensembl
Cytoband2q22.3
Allele length
AssemblyAllele length
hg383518
hg193518
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3114842
Supporting Variants
Samplessample149
Known GenesZEB2
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14104692
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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