A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6390093



Internal ID21047646
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:98091967..98547758hg38UCSC Ensembl
chr4:99013118..99468909hg19UCSC Ensembl
Cytoband4q23
Allele length
AssemblyAllele length
hg38455792
hg19455792
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18214398
Samples
Known GenesRAP1GDS1, STPG2, TSPAN5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6390093
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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