A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6362941



Internal ID21020494
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:180032101..180044100hg38UCSC Ensembl
chr3:179749889..179761888hg19UCSC Ensembl
Cytoband3q26.33
Allele length
AssemblyAllele length
hg3812000
hg1912000
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18211521
Samples
Known GenesPEX5L
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6362941
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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