A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6587968



Internal ID20961039
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:123077548..123078076hg38UCSC Ensembl
chr11:122948256..122948784hg19UCSC Ensembl
Cytoband11q24.1
Allele length
AssemblyAllele length
hg38529
hg19529
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18219049
Samples
Known GenesCLMP
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6587968
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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