A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14104756



Internal ID21271184
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:35591980..35748315hg38UCSC Ensembl
Innerchr2:35817046..35973381hg19UCSC Ensembl
Cytoband2p22.3
Allele length
AssemblyAllele length
hg38156336
hg19156336
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3115037
Supporting Variants
Samplessample160
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14104756
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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