A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18269233



Internal ID20836273
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:120396176..120949717hg38UCSC Ensembl
chr6:120717322..121270863hg19UCSC Ensembl
Cytoband6q22.31
Allele length
AssemblyAllele length
hg38553542
hg19553542
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6557210
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18269233
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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