A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14100600



Internal ID21277562
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 StatusS
Merged Variantsnsv3111849
Supporting Variants
Samplessample253
Known GenesWDR88
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14100600
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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