A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6576191



Internal ID20949262
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:45494256..45494714hg38UCSC Ensembl
chr13:46068391..46068849hg19UCSC Ensembl
Cytoband13q14.13
Allele length
AssemblyAllele length
hg38459
hg19459
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18232251
Samples
Known GenesCOG3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6576191
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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