A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5978690



Internal ID22753625
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:58000184..58217938hg38UCSC Ensembl
chr11:57767656..57985410hg19UCSC Ensembl
Cytoband11q12.1
Allele length
AssemblyAllele length
hg38217755
hg19217755
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17363363
Samples
Known GenesOR1S1, OR1S2, OR6Q1, OR9I1, OR9Q1, OR9Q2
MethodSequencing
Analysis
Platform
CommentsDESC=[BREAKPOINT1]
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5978690
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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