A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6590262



Internal ID20963333
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:5786169..5868284hg38UCSC Ensembl
chr11:5807399..5889514hg19UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg3882116
hg1982116
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18228971
Samples
Known GenesOR52E6, OR52E8, OR52N1, OR52N2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6590262
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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