A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6358222



Internal ID21015775
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:22630896..22855057hg38UCSC Ensembl
chr3:22672387..22896548hg19UCSC Ensembl
Cytoband3p24.3
Allele length
AssemblyAllele length
hg38224162
hg19224162
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18210414
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6358222
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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