A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6585047



Internal ID20958118
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:6453491..6459822hg38UCSC Ensembl
chr18:6453490..6459821hg19UCSC Ensembl
Cytoband18p11.31
Allele length
AssemblyAllele length
hg386332
hg196332
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18245489
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6585047
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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