A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6367806



Internal ID21025359
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:118715401..118723200hg38UCSC Ensembl
chr3:118434248..118442047hg19UCSC Ensembl
Cytoband3q13.32
Allele length
AssemblyAllele length
hg387800
hg197800
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4987n223
Supporting Variantsnssv18207893
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6367806
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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