A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6579549



Internal ID20952620
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:90334406..90334962hg38UCSC Ensembl
chr13:90986660..90987216hg19UCSC Ensembl
Cytoband13q31.3
Allele length
AssemblyAllele length
hg38557
hg19557
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18227027
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6579549
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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