A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6366484



Internal ID21024037
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:107517401..107522600hg38UCSC Ensembl
chr3:107236248..107241447hg19UCSC Ensembl
Cytoband3q13.12
Allele length
AssemblyAllele length
hg385200
hg195200
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18207203
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6366484
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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