A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5458036



Internal ID236069
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:76661863..76664836hg38UCSC Ensembl
chr6:77371580..77374553hg19UCSC Ensembl
Cytoband6q14.1
Allele length
AssemblyAllele length
hg382974
hg192974
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16983804
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5458036
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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