A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18198291



Internal ID20765331
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:50824801..50829800hg38UCSC Ensembl
chr19:51328057..51333056hg19UCSC Ensembl
Cytoband19q13.33
Allele length
AssemblyAllele length
hg385000
hg195000
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6533362
Supporting Variants
Samples
Known GenesKLK15
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18198291
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00019


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