A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6574747



Internal ID20947818
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:18467621..18468429hg38UCSC Ensembl
chr5:18467730..18468538hg19UCSC Ensembl
Cytoband5p14.3
Allele length
AssemblyAllele length
hg38809
hg19809
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18268269
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6574747
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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