A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6588626



Internal ID20961697
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:8492985..8493790hg38UCSC Ensembl
chr18:8492983..8493788hg19UCSC Ensembl
Cytoband18p11.23
Allele length
AssemblyAllele length
hg38806
hg19806
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18244866
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6588626
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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