A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6584591



Internal ID20957662
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:50807955..50808562hg38UCSC Ensembl
chr18:48334325..48334932hg19UCSC Ensembl
Cytoband18q21.2
Allele length
AssemblyAllele length
hg38608
hg19608
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18246958
Samples
Known GenesMRO
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6584591
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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