A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6586282



Internal ID20959353
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:60454875..60456081hg38UCSC Ensembl
chr13:61029009..61030215hg19UCSC Ensembl
Cytoband13q21.2
Allele length
AssemblyAllele length
hg381207
hg191207
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18230808
Samples
Known GenesTDRD3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6586282
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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