A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16989559



Internal ID60466
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:145862340..145862829hg38UCSC Ensembl
chr6:146183476..146183965hg19UCSC Ensembl
Cytoband6q24.3
Allele length
AssemblyAllele length
hg38490
hg19490
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5454672
Supporting Variants
Samples
Known GenesLOC100507557
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16989559
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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