A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17355771



Internal ID22581440
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:2318049..2319822hg38UCSC Ensembl
chr11:2339279..2341052hg19UCSC Ensembl
Cytoband11p15.5
Allele length
AssemblyAllele length
hg381774
hg191774
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5968630
Supporting Variants
Samples
Known GenesTSPAN32
MethodSequencing
Analysis
Platform
CommentsDESC=[BREAKPOINT1]
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17355771
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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