A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17540168



Internal ID21864523
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 StatusS
Merged Variantsnsv6102820
Supporting Variants
Samples
Known GenesFAM13B, MYOT, PKD2L2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17540168
Frequency
Sample Size405
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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