A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16980804



Internal ID54570
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:24698776..24699380hg38UCSC Ensembl
chr6:24699004..24699608hg19UCSC Ensembl
Cytoband6p22.3
Allele length
AssemblyAllele length
hg38605
hg19605
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5457029
Supporting Variants
Samples
Known GenesACOT13
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16980804
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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