A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6581424



Internal ID20954495
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:73566484..73567177hg38UCSC Ensembl
chr10:75326242..75326935hg19UCSC Ensembl
Cytoband10q22.2
Allele length
AssemblyAllele length
hg38694
hg19694
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18220073
Samples
Known GenesUSP54
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6581424
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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