A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14101460



Internal ID21283610
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:34923336..34924484hg38UCSC Ensembl
Innerchr19:35414240..35415388hg19UCSC Ensembl
Cytoband19q13.11
Allele length
AssemblyAllele length
hg381149
hg191149
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3114275
Supporting Variants
Samplessample347
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14101460
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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