A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6584292



Internal ID20957363
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:60557157..60557850hg38UCSC Ensembl
chr13:61131291..61131984hg19UCSC Ensembl
Cytoband13q21.2
Allele length
AssemblyAllele length
hg38694
hg19694
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18232728
Samples
Known GenesTDRD3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6584292
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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