A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18222195



Internal ID20789235
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:45989496..45990313hg38UCSC Ensembl
chr11:46011047..46011864hg19UCSC Ensembl
Cytoband11p11.2
Allele length
AssemblyAllele length
hg38818
hg19818
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6576322
Supporting Variants
Samples
Known GenesPHF21A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18222195
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00014


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