A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6587577



Internal ID20960648
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:116769808..116770730hg38UCSC Ensembl
chr11:116640524..116641446hg19UCSC Ensembl
Cytoband11q23.3
Allele length
AssemblyAllele length
hg38923
hg19923
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18223645
Samples
Known GenesBUD13
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6587577
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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