A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18198096



Internal ID20765136
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:3800539..3847282hg38UCSC Ensembl
chr19:3800537..3847280hg19UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg3846744
hg1946744
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6519310
Supporting Variants
Samples
Known GenesMATK, ZFR2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18198096
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00046


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