A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18197694



Internal ID20764734
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:17331894..17339726hg38UCSC Ensembl
chr19:17442703..17450535hg19UCSC Ensembl
Cytoband19p13.11
Allele length
AssemblyAllele length
hg387833
hg197833
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6522453
Supporting Variants
Samples
Known GenesANO8, GTPBP3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18197694
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.01568


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