A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14101053



Internal ID21279258
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 StatusS
Merged Variantsnsv3113018
Supporting Variants
Samplessample28
Known GenesHKR1
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14101053
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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