A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6594777



Internal ID20967848
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:104930881..106737596hg38UCSC Ensembl
chr13:105583232..107389944hg19UCSC Ensembl
Cytoband13q33.2
Allele length
AssemblyAllele length
hg381806716
hg191806713
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18231054
Samples
Known GenesARGLU1, DAOA, DAOA-AS1, EFNB2, LINC00343, LINC00443, LINC00460, LINC00551
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6594777
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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