A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6569462



Internal ID20942533
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:123290013..123292571hg38UCSC Ensembl
chr6:123611158..123613716hg19UCSC Ensembl
Cytoband6q22.31
Allele length
AssemblyAllele length
hg382559
hg192559
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18271134
Samples
Known GenesTRDN
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6569462
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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