A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6590499



Internal ID20963570
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:59460761..59461998hg38UCSC Ensembl
chr18:57127993..57129230hg19UCSC Ensembl
Cytoband18q21.32
Allele length
AssemblyAllele length
hg381238
hg191238
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18245390
Samples
Known GenesCCBE1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6590499
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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