A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6559413



Internal ID20932484
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:133040832..133058961hg38UCSC Ensembl
chr6:133361971..133380100hg19UCSC Ensembl
Cytoband6q23.2
Allele length
AssemblyAllele length
hg3818130
hg1918130
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18271904
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6559413
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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