A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5969946



Internal ID22744881
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:114204461..114260501hg38UCSC Ensembl
chr11:114075183..114131223hg19UCSC Ensembl
Cytoband11q23.2
Allele length
AssemblyAllele length
hg3856041
hg1956041
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17364769
Samples
Known GenesZBTB16
MethodSequencing
Analysis
Platform
CommentsDESC=[BREAKPOINT1]
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5969946
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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