A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6110917



Internal ID22020150
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:50029587..50151310hg38UCSC Ensembl
chr10:51789347..51911070hg19UCSC Ensembl
Cytoband10q11.23
Allele length
AssemblyAllele length
hg38121724
hg19121724
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17591538
Samples
Known GenesFAM21A, FAM21B, FLJ31813
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6110917
Frequency
Sample Size405
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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