A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14099663



Internal ID21269069
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:52385540..52390472hg38UCSC Ensembl
Innerchr19:52888793..52893725hg19UCSC Ensembl
Cytoband19q13.41
Allele length
AssemblyAllele length
hg384933
hg194933
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3115888
Supporting Variants
Samplessample134
Known GenesZNF880
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14099663
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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