A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6373478



Internal ID21031031
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:165232472..165232982hg38UCSC Ensembl
chr3:164950260..164950770hg19UCSC Ensembl
Cytoband3q26.1
Allele length
AssemblyAllele length
hg38511
hg19511
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18208521
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6373478
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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