A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6370290



Internal ID21027843
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:20791501..20798300hg38UCSC Ensembl
chr3:20832993..20839792hg19UCSC Ensembl
Cytoband3p24.3
Allele length
AssemblyAllele length
hg386800
hg196800
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18098533
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6370290
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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