A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6586517



Internal ID20959588
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:28720479..28721283hg38UCSC Ensembl
chr13:29294616..29295420hg19UCSC Ensembl
Cytoband13q12.3
Allele length
AssemblyAllele length
hg38805
hg19805
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18234421
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6586517
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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