A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5457918



Internal ID235953
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:80636513..80666767hg38UCSC Ensembl
chr6:81346230..81376484hg19UCSC Ensembl
Cytoband6q14.1
Allele length
AssemblyAllele length
hg3830255
hg1930255
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16985722
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5457918
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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