A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18217865



Internal ID20784905
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:112065087..112065896hg38UCSC Ensembl
chr11:111935811..111936620hg19UCSC Ensembl
Cytoband11q23.1
Allele length
AssemblyAllele length
hg38810
hg19810
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6579330
Supporting Variants
Samples
Known GenesPIH1D2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18217865
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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