A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18197774



Internal ID20764814
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:35349301..35364800hg38UCSC Ensembl
chr19:35840204..35855702hg19UCSC Ensembl
Cytoband19q13.12
Allele length
AssemblyAllele length
hg3815500
hg1915499
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6533085
Supporting Variants
Samples
Known GenesFFAR1, FFAR3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18197774
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.0001


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