A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18220330



Internal ID20787370
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:73587361..73587876hg38UCSC Ensembl
chr11:73298406..73298921hg19UCSC Ensembl
Cytoband11q13.4
Allele length
AssemblyAllele length
hg38516
hg19516
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6586076
Supporting Variants
Samples
Known GenesFAM168A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18220330
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00017


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