A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18198835



Internal ID20765875
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:44065616..44073582hg38UCSC Ensembl
chr19:44569769..44577735hg19UCSC Ensembl
Cytoband19q13.31
Allele length
AssemblyAllele length
hg387967
hg197967
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6528000
Supporting Variants
Samples
Known GenesZNF223, ZNF284
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18198835
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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