A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6583465



Internal ID20956536
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:50859069..50859528hg38UCSC Ensembl
chr18:48385439..48385898hg19UCSC Ensembl
Cytoband18q21.2
Allele length
AssemblyAllele length
hg38460
hg19460
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18246963
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6583465
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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