A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17594639



Internal ID21786682
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:73984249..73989663hg38UCSC Ensembl
chr11:73695294..73700708hg19UCSC Ensembl
Cytoband11q13.4
Allele length
AssemblyAllele length
hg385415
hg195415
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6110903
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17594639
Frequency
Sample Size405
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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