A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18228030



Internal ID20795070
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:117173637..117179147hg38UCSC Ensembl
chr11:117044353..117049863hg19UCSC Ensembl
Cytoband11q23.3
Allele length
AssemblyAllele length
hg385511
hg195511
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6582537
Supporting Variants
Samples
Known GenesPAFAH1B2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18228030
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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