A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6569190



Internal ID20942261
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:55630313..55630715hg38UCSC Ensembl
chr5:54926141..54926543hg19UCSC Ensembl
Cytoband5q11.2
Allele length
AssemblyAllele length
hg38403
hg19403
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18269093
Samples
Known GenesSLC38A9
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6569190
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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