A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18267973



Internal ID20835013
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:143225433..143226217hg38UCSC Ensembl
chr5:142604998..142605782hg19UCSC Ensembl
Cytoband5q31.3
Allele length
AssemblyAllele length
hg38785
hg19785
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6570169
Supporting Variants
Samples
Known GenesARHGAP26
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18267973
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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