A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6567389



Internal ID20940460
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:110375238..110376028hg38UCSC Ensembl
chr4:111296394..111297184hg19UCSC Ensembl
Cytoband4q25
Allele length
AssemblyAllele length
hg38791
hg19791
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18263588
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6567389
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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