A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16990968



Internal ID61391
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:166052616..166055808hg38UCSC Ensembl
chr6:166466104..166469296hg19UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg383193
hg193193
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5473305
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16990968
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000312


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