A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6569403



Internal ID20942474
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:1451620..1524547hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg3872928
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18264776
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6569403
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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