A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18236496



Internal ID20803536
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:106058102..106058644hg38UCSC Ensembl
chr11:105928829..105929371hg19UCSC Ensembl
Cytoband11q22.3
Allele length
AssemblyAllele length
hg38543
hg19543
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6588662
Supporting Variants
Samples
Known GenesKBTBD3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18236496
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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