A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14105038



Internal ID21267191
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:77001393..77006219hg38UCSC Ensembl
Innerchr2:77228519..77233345hg19UCSC Ensembl
Cytoband2p12
Allele length
AssemblyAllele length
hg384827
hg194827
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3118286
Supporting Variants
Samplessample11
Known GenesLRRTM4
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14105038
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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