A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5468281



Internal ID246082
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:158731205..158736189hg38UCSC Ensembl
chr6:159152237..159157221hg19UCSC Ensembl
Cytoband6q25.3
Allele length
AssemblyAllele length
hg384985
hg194985
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16989518
Samples
Known GenesSYTL3
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5468281
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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