A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18197333



Internal ID20764373
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:11808748..11848070hg38UCSC Ensembl
chr19:11919563..11958885hg19UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg3839323
hg1939323
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6521792
Supporting Variants
Samples
Known GenesZNF440
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18197333
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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