A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5464182



Internal ID242062
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:92812529..92812593hg38UCSC Ensembl
chr6:93522247..93522311hg19UCSC Ensembl
Cytoband6q16.1
Allele length
AssemblyAllele length
hg3865
hg1965
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16986914
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5464182
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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