A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6595426



Internal ID20968497
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:25656508..25656648hg38UCSC Ensembl
chr18:23236472..23236612hg19UCSC Ensembl
Cytoband18q11.2
Allele length
AssemblyAllele length
hg38141
hg19141
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18246837
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6595426
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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