A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14106980



Internal ID21288263
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:209458812..209463887hg38UCSC Ensembl
Innerchr2:210323536..210328611hg19UCSC Ensembl
Cytoband2q34
Allele length
AssemblyAllele length
hg385076
hg195076
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3115685
Supporting Variants
Samplessample414
Known GenesMAP2
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14106980
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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