A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16970350



Internal ID47559
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:142905796..142908761hg38UCSC Ensembl
chr6:143226933..143229898hg19UCSC Ensembl
Cytoband6q24.2
Allele length
AssemblyAllele length
hg382966
hg192966
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5471280
Supporting Variants
Samples
Known GenesHIVEP2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16970350
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.001718


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