A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6570169



Internal ID20943240
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 StatusM
Merged Variants
Supporting Variantsnssv18267973
Samples
Known GenesARHGAP26
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6570169
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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