A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18198072



Internal ID20765112
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:11804145..11953016hg38UCSC Ensembl
chr19:11914960..12063831hg19UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg38148872
hg19148872
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6516815
Supporting Variants
Samples
Known GenesZNF439, ZNF440, ZNF491, ZNF69, ZNF700
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18198072
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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