A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6577583



Internal ID20950654
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:45868373..45868885hg38UCSC Ensembl
chr18:43448338..43448850hg19UCSC Ensembl
Cytoband18q12.3
Allele length
AssemblyAllele length
hg38513
hg19513
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3359n223
Supporting Variantsnssv18246869
Samples
Known GenesEPG5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6577583
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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