A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6586779



Internal ID20959850
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:77944136..77945183hg38UCSC Ensembl
chr10:79703894..79704941hg19UCSC Ensembl
Cytoband10q22.3
Allele length
AssemblyAllele length
hg381048
hg191048
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18235816
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6586779
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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