A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5973995



Internal ID22748930
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 StatusM
Merged Variants
Supporting Variantsnssv17391559
Samples
Known GenesLINC00654
MethodSequencing
Analysis
Platform
CommentsDESC=[BREAKPOINT2]
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5973995
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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