A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16988674



Internal ID59873
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:106047145..106058606hg38UCSC Ensembl
chr6:106495020..106506481hg19UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg3811462
hg1911462
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5461218
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16988674
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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