A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6585219



Internal ID20958290
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:6302833..6303287hg38UCSC Ensembl
chr18:6302832..6303286hg19UCSC Ensembl
Cytoband18p11.31
Allele length
AssemblyAllele length
hg38455
hg19455
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18245468
Samples
Known GenesL3MBTL4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6585219
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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