A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6366833



Internal ID21024386
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:46587879..46590070hg38UCSC Ensembl
chr3:46629369..46631560hg19UCSC Ensembl
Cytoband3p21.31
Allele length
AssemblyAllele length
hg382192
hg192192
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18100715
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6366833
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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