A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6579378



Internal ID20952449
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:56157251..56157390hg38UCSC Ensembl
chr13:56731385..56731524hg19UCSC Ensembl
Cytoband13q21.1
Allele length
AssemblyAllele length
hg38140
hg19140
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18229826
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6579378
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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