A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6364314



Internal ID21021867
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:69322845..69344695hg38UCSC Ensembl
chr3:69371996..69393846hg19UCSC Ensembl
Cytoband3p14.1
Allele length
AssemblyAllele length
hg3821851
hg1921851
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18211222
Samples
Known GenesFRMD4B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6364314
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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