A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16986421



Internal ID58382
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 StatusS
Merged Variantsnsv6147343
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16986421
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.075242


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