A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6358961



Internal ID21016514
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:166847333..166864903hg38UCSC Ensembl
chr3:166565121..166582691hg19UCSC Ensembl
Cytoband3q26.1
Allele length
AssemblyAllele length
hg3817571
hg1917571
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18098696
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6358961
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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