A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18230299



Internal ID20797339
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:75646540..75647252hg38UCSC Ensembl
chr11:75357585..75358297hg19UCSC Ensembl
Cytoband11q13.5
Allele length
AssemblyAllele length
hg38713
hg19713
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6595007
Supporting Variants
Samples
Known GenesMAP6
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18230299
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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