A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6579977



Internal ID20953048
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:80347368..80347995hg38UCSC Ensembl
chr13:80921503..80922130hg19UCSC Ensembl
Cytoband13q31.1
Allele length
AssemblyAllele length
hg38628
hg19628
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1923n223
Supporting Variantsnssv18217938
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6579977
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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