A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16989558



Internal ID60465
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:145823348..145827725hg38UCSC Ensembl
chr6:146144484..146148861hg19UCSC Ensembl
Cytoband6q24.3
Allele length
AssemblyAllele length
hg384378
hg194378
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5463607
Supporting Variants
Samples
Known GenesLOC100507557
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16989558
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000781


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