A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6370436



Internal ID21027989
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:45223901..45227100hg38UCSC Ensembl
chr3:45265393..45268592hg19UCSC Ensembl
Cytoband3p21.31
Allele length
AssemblyAllele length
hg383200
hg193200
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18209274
Samples
Known GenesTMEM158
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6370436
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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