A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3117019



Internal ID21300285
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:9168914..9179255hg38UCSC Ensembl
Innerchr19:9279590..9289931hg19UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg3810342
hg1910342
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14100593
Samplessample250
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3117019
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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