A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14103355



Internal ID21288968
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:99487248..99490863hg38UCSC Ensembl
Innerchr2:100103710..100107325hg19UCSC Ensembl
Cytoband2q11.2
Allele length
AssemblyAllele length
hg383616
hg193616
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3117127
Supporting Variants
Samplessample424
Known GenesREV1
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14103355
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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