A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6360489



Internal ID21018042
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:69271193..69294470hg38UCSC Ensembl
chr3:69320344..69343621hg19UCSC Ensembl
Cytoband3p14.1
Allele length
AssemblyAllele length
hg3823278
hg1923278
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18211221
Samples
Known GenesFRMD4B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6360489
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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