A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18220165



Internal ID20787205
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:61391274..61391747hg38UCSC Ensembl
chr11:61158746..61159219hg19UCSC Ensembl
Cytoband11q12.2
Allele length
AssemblyAllele length
hg38474
hg19474
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6580908
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18220165
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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