A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18271985



Internal ID20839025
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:45914801..45915217hg38UCSC Ensembl
chr6:45882538..45882954hg19UCSC Ensembl
Cytoband6p21.1
Allele length
AssemblyAllele length
hg38417
hg19417
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6572771
Supporting Variants
Samples
Known GenesCLIC5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18271985
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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