A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6374886



Internal ID21032439
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:22990717..22994802hg38UCSC Ensembl
chr3:23032208..23036293hg19UCSC Ensembl
Cytoband3p24.3
Allele length
AssemblyAllele length
hg384086
hg194086
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18100331
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6374886
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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