A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17391559



Internal ID22449429
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:5504284..5537063hg38UCSC Ensembl
chr20:5484930..5517709hg19UCSC Ensembl
Cytoband20p12.3
Allele length
AssemblyAllele length
hg3832780
hg1932780
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5973995
Supporting Variants
Samples
Known GenesLINC00654
MethodSequencing
Analysis
Platform
CommentsDESC=[BREAKPOINT2]
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17391559
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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