A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17604884



Internal ID21796931
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:123108263..123124373hg38UCSC Ensembl
chr11:122978971..122995081hg19UCSC Ensembl
Cytoband11q24.1
Allele length
AssemblyAllele length
hg3816111
hg1916111
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6110180
Supporting Variants
Samples
Known GenesCLMP
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17604884
Frequency
Sample Size405
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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