A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16991175



Internal ID61520
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:162772680..162931718hg38UCSC Ensembl
chr6:163193712..163352750hg19UCSC Ensembl
Cytoband6q26
Allele length
AssemblyAllele length
hg38159039
hg19159039
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5457281
Supporting Variants
Samples
Known GenesPACRG
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16991175
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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