A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6574123



Internal ID20947194
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:139615430..139615999hg38UCSC Ensembl
chr5:138995015..138995584hg19UCSC Ensembl
Cytoband5q31.2
Allele length
AssemblyAllele length
hg38570
hg19570
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18266877
Samples
Known GenesUBE2D2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6574123
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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