A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18219725



Internal ID20786765
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:45781094..45781606hg38UCSC Ensembl
chr11:45802645..45803157hg19UCSC Ensembl
Cytoband11p11.2
Allele length
AssemblyAllele length
hg38513
hg19513
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6575635
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18219725
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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