A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16980128



Internal ID54132
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:24044690..24045305hg38UCSC Ensembl
chr6:24044918..24045533hg19UCSC Ensembl
Cytoband6p22.3
Allele length
AssemblyAllele length
hg38616
hg19616
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5562349
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16980128
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.000156


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