A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17582629



Internal ID21774672
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:65757441..65758195hg38UCSC Ensembl
chr11:65524912..65525666hg19UCSC Ensembl
Cytoband11q13.1
Allele length
AssemblyAllele length
hg38755
hg19755
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6108169
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17582629
Frequency
Sample Size405
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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