A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18198833



Internal ID20765873
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:43707730..43741488hg38UCSC Ensembl
chr19:44211882..44245640hg19UCSC Ensembl
Cytoband19q13.31
Allele length
AssemblyAllele length
hg3833759
hg1933759
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6524479
Supporting Variants
Samples
Known GenesIRGC, SMG9
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18198833
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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