A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5973850



Internal ID22748785
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:66252469..66253352hg38UCSC Ensembl
chr11:66019940..66020823hg19UCSC Ensembl
Cytoband11q13.2
Allele length
AssemblyAllele length
hg38884
hg19884
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17355332
Samples
Known Genes
MethodSequencing
Analysis
Platform
CommentsDESC=[BREAKPOINT2]
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5973850
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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