A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18198840



Internal ID20765880
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:44291798..44336656hg38UCSC Ensembl
chr19:44795951..44840809hg19UCSC Ensembl
Cytoband19q13.31
Allele length
AssemblyAllele length
hg3844859
hg1944859
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6531986
Supporting Variants
Samples
Known GenesZNF112, ZNF235
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18198840
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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