A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6583705



Internal ID20956776
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:108918716..108920450hg38UCSC Ensembl
chr13:109571064..109572798hg19UCSC Ensembl
Cytoband13q33.3
Allele length
AssemblyAllele length
hg381735
hg191735
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18224660
Samples
Known GenesMYO16
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6583705
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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