A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6583241



Internal ID20956312
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:45496773..45497506hg38UCSC Ensembl
chr13:46070908..46071641hg19UCSC Ensembl
Cytoband13q14.13
Allele length
AssemblyAllele length
hg38734
hg19734
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18236267
Samples
Known GenesCOG3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6583241
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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