A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14105761



Internal ID21275604
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:136509321..136511430hg38UCSC Ensembl
Innerchr2:137266891..137269000hg19UCSC Ensembl
Cytoband2q22.1
Allele length
AssemblyAllele length
hg382110
hg192110
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3118244
Supporting Variants
Samplessample225
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14105761
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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