A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5970522



Internal ID22745457
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:80283200..80284604hg38UCSC Ensembl
chr11:79994244..79995648hg19UCSC Ensembl
Cytoband11q14.1
Allele length
AssemblyAllele length
hg381405
hg191405
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17366534
Samples
Known Genes
MethodSequencing
Analysis
Platform
CommentsDESC=[BREAKPOINT1]
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5970522
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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