A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6147343



Internal ID346524
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:111903222..111908454hg38UCSC Ensembl
chr6:112224425..112229657hg19UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg385233
hg195233
Variant TypeCNV mobile element deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16986421
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv6147343
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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