A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3114914



Internal ID21298180
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:12619373..12624463hg38UCSC Ensembl
Innerchr19:12730187..12735277hg19UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg385091
hg195091
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14101906
Samplessample102
Known GenesZNF791
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3114914
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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