A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6592379



Internal ID20965450
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:80347298..80348042hg38UCSC Ensembl
chr13:80921433..80922177hg19UCSC Ensembl
Cytoband13q31.1
Allele length
AssemblyAllele length
hg38745
hg19745
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1923n223
Supporting Variantsnssv18226769
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6592379
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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