A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6593974



Internal ID20967045
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:117264834..117265471hg38UCSC Ensembl
chr11:117135550..117136187hg19UCSC Ensembl
Cytoband11q23.3
Allele length
AssemblyAllele length
hg38638
hg19638
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18228322
Samples
Known GenesRNF214
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6593974
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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