A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5974880



Internal ID22749815
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:15786465..15790198hg38UCSC Ensembl
chr11:15808011..15811744hg19UCSC Ensembl
Cytoband11p15.2
Allele length
AssemblyAllele length
hg383734
hg193734
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17352367
Samples
Known Genes
MethodSequencing
Analysis
Platform
CommentsDESC=[BREAKPOINT1]
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5974880
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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