A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6589763



Internal ID20962834
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:73369621..73370490hg38UCSC Ensembl
chr13:73943758..73944627hg19UCSC Ensembl
Cytoband13q22.1
Allele length
AssemblyAllele length
hg38870
hg19870
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18223376
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6589763
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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