A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6580799



Internal ID20953870
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:53545453..53546093hg38UCSC Ensembl
chr18:51071823..51072463hg19UCSC Ensembl
Cytoband18q21.2
Allele length
AssemblyAllele length
hg38641
hg19641
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18244668
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6580799
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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