A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6579115



Internal ID20952186
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:111374003..111377861hg38UCSC Ensembl
chr13:112026350..112030208hg19UCSC Ensembl
Cytoband13q34
Allele length
AssemblyAllele length
hg383859
hg193859
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18237052
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6579115
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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