A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5467347



Internal ID245162
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:111511074..111511127hg38UCSC Ensembl
chr6:111832277..111832330hg19UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg3854
hg1954
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16988756
Samples
Known GenesTRAF3IP2-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5467347
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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