A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18198939



Internal ID20765979
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:4716485..4746721hg38UCSC Ensembl
chr19:4716497..4746733hg19UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg3830237
hg1930237
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6522295
Supporting Variants
Samples
Known GenesDPP9
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18198939
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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