A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14106157



Internal ID21281798
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:102201996..102223451hg38UCSC Ensembl
Innerchr2:102818456..102839911hg19UCSC Ensembl
Cytoband2q12.1
Allele length
AssemblyAllele length
hg3821456
hg1921456
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3117763
Supporting Variants
Samplessample318
Known GenesIL1RL2
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14106157
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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