A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6587614



Internal ID20960685
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:63296410..63297074hg38UCSC Ensembl
chr18:60963643..60964307hg19UCSC Ensembl
Cytoband18q21.33
Allele length
AssemblyAllele length
hg38665
hg19665
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18245472
Samples
Known GenesBCL2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6587614
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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