A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6586927



Internal ID20959998
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:6091293..6098786hg38UCSC Ensembl
chr18:6091292..6098785hg19UCSC Ensembl
Cytoband18p11.31
Allele length
AssemblyAllele length
hg387494
hg197494
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3273n223
Supporting Variantsnssv18245424
Samples
Known GenesL3MBTL4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6586927
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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