A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6580344



Internal ID20953415
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:54577611..54578827hg38UCSC Ensembl
chr18:52244842..52246058hg19UCSC Ensembl
Cytoband18q21.2
Allele length
AssemblyAllele length
hg381217
hg191217
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3373n223
Supporting Variantsnssv18244680
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6580344
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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