A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5973282



Internal ID22748217
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:15269912..16720775hg38UCSC Ensembl
chr11:15291458..16742322hg19UCSC Ensembl
Cytoband11p15.1
Allele length
AssemblyAllele length
hg381450864
hg191450865
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17368040
Samples
Known GenesSOX6
MethodSequencing
Analysis
Platform
CommentsDESC=[BREAKPOINT1]
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5973282
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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