A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6575998



Internal ID20949069
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:126040920..126041906hg38UCSC Ensembl
chr11:125910815..125911801hg19UCSC Ensembl
Cytoband11q24.2
Allele length
AssemblyAllele length
hg38987
hg19987
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18223202
Samples
Known GenesCDON
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6575998
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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