A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6594554



Internal ID20967625
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:61899884..61900541hg38UCSC Ensembl
chr18:59567117..59567774hg19UCSC Ensembl
Cytoband18q21.33
Allele length
AssemblyAllele length
hg38658
hg19658
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18244720
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6594554
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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