A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6595074



Internal ID20968145
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:108151356..108152203hg38UCSC Ensembl
chr11:108022083..108022930hg19UCSC Ensembl
Cytoband11q22.3
Allele length
AssemblyAllele length
hg38848
hg19848
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18224993
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6595074
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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