A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16987884



Internal ID59359
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:107297336..107302499hg38UCSC Ensembl
chr6:107618540..107623703hg19UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg385164
hg195164
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5470311
Supporting Variants
Samples
Known GenesPDSS2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16987884
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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