A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6102820



Internal ID22012055
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:137882518..138014246hg38UCSC Ensembl
chr5:137218207..137349935hg19UCSC Ensembl
Cytoband5q31.2
Allele length
AssemblyAllele length
hg38131729
hg19131729
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17540168
Samples
Known GenesFAM13B, MYOT, PKD2L2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6102820
Frequency
Sample Size405
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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