A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6590033



Internal ID20963104
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:45807747..45807852hg38UCSC Ensembl
chr13:46381882..46381987hg19UCSC Ensembl
Cytoband13q14.13
Allele length
AssemblyAllele length
hg38106
hg19106
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18225350
Samples
Known GenesSIAH3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6590033
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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