A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18234757



Internal ID20801797
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:86572024..86577793hg38UCSC Ensembl
chr11:86283066..86288835hg19UCSC Ensembl
Cytoband11q14.2
Allele length
AssemblyAllele length
hg385770
hg195770
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6577394
Supporting Variants
Samples
Known GenesME3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18234757
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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