A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3113018



Internal ID21296284
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:37349597..37355511hg38UCSC Ensembl
Innerchr19:37840499..37846413hg19UCSC Ensembl
Cytoband19q13.12
Allele length
AssemblyAllele length
hg385915
hg195915
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14101053
Samplessample28
Known GenesHKR1
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3113018
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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