A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5968465



Internal ID22743400
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:101251731..101252553hg38UCSC Ensembl
chr11:101122462..101123284hg19UCSC Ensembl
Cytoband11q22.1
Allele length
AssemblyAllele length
hg38823
hg19823
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17356274
Samples
Known Genes
MethodSequencing
Analysis
Platform
CommentsDESC=[BREAKPOINT1]
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5968465
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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