A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6362098



Internal ID21019651
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:40328071..40332719hg38UCSC Ensembl
chr3:40369562..40374210hg19UCSC Ensembl
Cytoband3p22.1
Allele length
AssemblyAllele length
hg384649
hg194649
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18100935
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6362098
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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