A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18271125



Internal ID20838165
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:122563389..122569211hg38UCSC Ensembl
chr6:122884534..122890356hg19UCSC Ensembl
Cytoband6q22.31
Allele length
AssemblyAllele length
hg385823
hg195823
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6567097
Supporting Variants
Samples
Known GenesPKIB
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18271125
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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