A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6541809



Internal ID20915077
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:13755370..13758290hg38UCSC Ensembl
chr1:14081865..14084785hg19UCSC Ensembl
Cytoband1p36.21
Allele length
AssemblyAllele length
hg382921
hg192921
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18247009
Samples
Known GenesPRDM2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6541809
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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