A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14106994



Internal ID21288402
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:143835616..143837742hg38UCSC Ensembl
Innerchr2:144593185..144595311hg19UCSC Ensembl
Cytoband2q22.3
Allele length
AssemblyAllele length
hg382127
hg192127
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3116410
Supporting Variants
Samplessample417
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14106994
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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