A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5976571



Internal ID22751506
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:15856696..15881883hg38UCSC Ensembl
chr11:15878242..15903429hg19UCSC Ensembl
Cytoband11p15.2
Allele length
AssemblyAllele length
hg3825188
hg1925188
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17362785
Samples
Known Genes
MethodSequencing
Analysis
Platform
CommentsDESC=[BREAKPOINT1]
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5976571
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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