A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6579765



Internal ID20952836
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:117283654..117284805hg38UCSC Ensembl
chr11:117154370..117155521hg19UCSC Ensembl
Cytoband11q23.3
Allele length
AssemblyAllele length
hg381152
hg191152
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18235475
Samples
Known GenesRNF214
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6579765
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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