A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6370893



Internal ID21028446
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:5200167..5422074hg38UCSC Ensembl
chr3:5241852..5463760hg19UCSC Ensembl
Cytoband3p26.1
Allele length
AssemblyAllele length
hg38221908
hg19221909
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18209980
Samples
Known GenesEDEM1, MIR4790
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6370893
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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