A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6578287



Internal ID20951358
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:80292869..80293489hg38UCSC Ensembl
chr13:80867004..80867624hg19UCSC Ensembl
Cytoband13q31.1
Allele length
AssemblyAllele length
hg38621
hg19621
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18222029
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6578287
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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