A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6584889



Internal ID20957960
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:60424040..60424557hg38UCSC Ensembl
chr13:60998174..60998691hg19UCSC Ensembl
Cytoband13q21.2
Allele length
AssemblyAllele length
hg38518
hg19518
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18228247
Samples
Known GenesTDRD3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6584889
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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