A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16989654



Internal ID60526
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:149968869..150001337hg38UCSC Ensembl
chr6:150290005..150322473hg19UCSC Ensembl
Cytoband6q25.1
Allele length
AssemblyAllele length
hg3832469
hg1932469
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5560969
Supporting Variants
Samples
Known GenesRAET1K, ULBP1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16989654
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.000312


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