A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18233056



Internal ID20800096
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:118621181..118624038hg38UCSC Ensembl
chr11:118491896..118494755hg19UCSC Ensembl
Cytoband11q23.3
Allele length
AssemblyAllele length
hg382858
hg192860
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6580130
Supporting Variants
Samples
Known GenesPHLDB1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18233056
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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