A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5455799



Internal ID233871
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:4568500..4573500hg38UCSC Ensembl
chr6:4568734..4573734hg19UCSC Ensembl
Cytoband6p25.1
Allele length
AssemblyAllele length
hg385001
hg195001
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16979944
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5455799
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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