A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16986723



Internal ID58588
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:108466451..108471515hg38UCSC Ensembl
chr6:108787654..108792718hg19UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg385065
hg195065
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5454304
Supporting Variants
Samples
Known GenesLACE1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16986723
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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