A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6516661



Internal ID20890022
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 StatusM
Merged Variants
Supporting Variantsnssv18199031
Samples
Known GenesC19orf59, RETN, TRAPPC5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6516661
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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