A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18231202



Internal ID20798242
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:59701527..59702847hg38UCSC Ensembl
chr11:59469000..59470320hg19UCSC Ensembl
Cytoband11q12.1
Allele length
AssemblyAllele length
hg381321
hg191321
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6587517
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18231202
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00011


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