A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16970923



Internal ID47955
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:144224084..144235172hg38UCSC Ensembl
chr6:144545221..144556308hg19UCSC Ensembl
Cytoband6q24.2
Allele length
AssemblyAllele length
hg3811089
hg1911088
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5472850
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16970923
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000312


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