A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6362633



Internal ID21020186
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:95383001..95405100hg38UCSC Ensembl
chr3:95101845..95123944hg19UCSC Ensembl
Cytoband3q11.2
Allele length
AssemblyAllele length
hg3822100
hg1922100
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18211226
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6362633
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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