A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14105206



Internal ID21278502
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:204149347..204161181hg38UCSC Ensembl
Innerchr2:205014070..205025904hg19UCSC Ensembl
Cytoband2q33.3
Allele length
AssemblyAllele length
hg3811835
hg1911835
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3115076
Supporting Variants
Samplessample270
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14105206
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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