A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18198293



Internal ID20765333
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:50942995..51022105hg38UCSC Ensembl
chr19:51446251..51525361hg19UCSC Ensembl
Cytoband19q13.41
Allele length
AssemblyAllele length
hg3879111
hg1979111
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6525605
Supporting Variants
Samples
Known GenesKLK10, KLK5, KLK6, KLK7, KLK8, KLK9
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18198293
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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