A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18198049



Internal ID20765089
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:10883935..11045237hg38UCSC Ensembl
chr19:10994611..11155913hg19UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg38161303
hg19161303
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6520341
Supporting Variants
Samples
Known GenesC19orf52, CARM1, SMARCA4, YIPF2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18198049
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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