A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18198296



Internal ID20765336
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:51028561..51032634hg38UCSC Ensembl
chr19:51531817..51535890hg19UCSC Ensembl
Cytoband19q13.41
Allele length
AssemblyAllele length
hg384074
hg194074
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6529731
Supporting Variants
Samples
Known GenesKLK12
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18198296
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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