A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3114780



Internal ID21298046
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:57635140..57640632hg38UCSC Ensembl
Innerchr19:58146508..58152000hg19UCSC Ensembl
Cytoband19q13.43
Allele length
AssemblyAllele length
hg385493
hg195493
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14101024, nssv14099027
Samplessample15, sample424
Known GenesZNF211
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3114780
Frequency
Sample Size467
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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