A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3111849



Internal ID21295115
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:33132809..33165517hg38UCSC Ensembl
Innerchr19:33623715..33656423hg19UCSC Ensembl
Cytoband19q13.11
Allele length
AssemblyAllele length
hg3832709
hg1932709
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14100600
Samplessample253
Known GenesWDR88
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3111849
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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