A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14101940



Internal ID21267613
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:27994299..28065966hg38UCSC Ensembl
Innerchr19:28485206..28556873hg19UCSC Ensembl
Cytoband19q11
Allele length
AssemblyAllele length
hg3871668
hg1971668
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3117742
Supporting Variants
Samplessample114
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14101940
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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