A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6358868



Internal ID21016421
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:184728076..184729090hg38UCSC Ensembl
chr3:184445864..184446878hg19UCSC Ensembl
Cytoband3q27.1
Allele length
AssemblyAllele length
hg381015
hg191015
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18097627
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6358868
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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