A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6373068



Internal ID21030621
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:43916114..43973519hg38UCSC Ensembl
chr3:43957606..44015011hg19UCSC Ensembl
Cytoband3p21.33
Allele length
AssemblyAllele length
hg3857406
hg1957406
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18099983
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6373068
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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