A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16969148



Internal ID46758
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:131563677..131563801hg38UCSC Ensembl
chr6:131884817..131884941hg19UCSC Ensembl
Cytoband6q23.2
Allele length
AssemblyAllele length
hg38125
hg19125
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5559854
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16969148
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.663648


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