A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5979393



Internal ID22754328
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:80835951..81056247hg38UCSC Ensembl
chr11:80546994..80767290hg19UCSC Ensembl
Cytoband11q14.1
Allele length
AssemblyAllele length
hg38220297
hg19220297
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17359416
Samples
Known Genes
MethodSequencing
Analysis
Platform
CommentsDESC=[BREAKPOINT1]
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5979393
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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