A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6360939



Internal ID21018492
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:98976265..98993358hg38UCSC Ensembl
chr3:98695109..98712202hg19UCSC Ensembl
Cytoband3q12.1
Allele length
AssemblyAllele length
hg3817094
hg1917094
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18211298
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6360939
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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