A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18199706



Internal ID20766746
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:57477101..57482100hg38UCSC Ensembl
chr19:57988469..57993468hg19UCSC Ensembl
Cytoband19q13.43
Allele length
AssemblyAllele length
hg385000
hg195000
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6533731
Supporting Variants
Samples
Known GenesZNF772
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18199706
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00306


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