A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5967593



Internal ID22742528
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:56470155..56491365hg38UCSC Ensembl
chr11:56237631..56258841hg19UCSC Ensembl
Cytoband11q12.1
Allele length
AssemblyAllele length
hg3821211
hg1921211
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17367436
Samples
Known GenesOR5M3, OR5M8
MethodSequencing
Analysis
Platform
CommentsDESC=[BREAKPOINT2]
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5967593
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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