A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5978212



Internal ID22753147
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:115391425..115448789hg38UCSC Ensembl
chr11:115262143..115319508hg19UCSC Ensembl
Cytoband11q23.3
Allele length
AssemblyAllele length
hg3857365
hg1957366
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17352374
Samples
Known GenesCADM1
MethodSequencing
Analysis
Platform
CommentsDESC=[BREAKPOINT1]
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5978212
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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