A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6590854



Internal ID20963925
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:63540796..63541482hg38UCSC Ensembl
chr11:63308268..63308954hg19UCSC Ensembl
Cytoband11q12.3
Allele length
AssemblyAllele length
hg38687
hg19687
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18223553
Samples
Known GenesMIR3680-1, MIR3680-2, RARRES3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6590854
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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