A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16969141



Internal ID46753
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:131507269..131904335hg38UCSC Ensembl
chr6:131828409..132225475hg19UCSC Ensembl
Cytoband6q23.2
Allele length
AssemblyAllele length
hg38397067
hg19397067
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5561463
Supporting Variants
Samples
Known GenesARG1, CTAGE9, ENPP1, ENPP3, MED23, OR2A4
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16969141
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.030128


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