A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6372149



Internal ID21029702
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:4206187..4253714hg38UCSC Ensembl
chr3:4247871..4295398hg19UCSC Ensembl
Cytoband3p26.1
Allele length
AssemblyAllele length
hg3847528
hg1947528
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18208656
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6372149
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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