A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6359583



Internal ID21017136
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:5348052..5397605hg38UCSC Ensembl
chr3:5389737..5439291hg19UCSC Ensembl
Cytoband3p26.1
Allele length
AssemblyAllele length
hg3849554
hg1949555
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18101639
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6359583
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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