A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18199031



Internal ID20766071
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:7659061..7686708hg38UCSC Ensembl
chr19:7723947..7751594hg19UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg3827648
hg1927648
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6516661
Supporting Variants
Samples
Known GenesC19orf59, RETN, TRAPPC5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18199031
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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