A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6577037



Internal ID20950108
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:57463969..57468372hg38UCSC Ensembl
chr18:55131201..55135604hg19UCSC Ensembl
Cytoband18q21.31
Allele length
AssemblyAllele length
hg384404
hg194404
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18245349
Samples
Known GenesONECUT2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6577037
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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