A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6357474



Internal ID21015027
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:31646588..31647847hg38UCSC Ensembl
chr3:31688080..31689339hg19UCSC Ensembl
Cytoband3p23
Allele length
AssemblyAllele length
hg381260
hg191260
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18099346
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6357474
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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