A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6567374



Internal ID20940445
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:162441707..162572559hg38UCSC Ensembl
chr4:163362859..163493711hg19UCSC Ensembl
Cytoband4q32.2
Allele length
AssemblyAllele length
hg38130853
hg19130853
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18264304
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6567374
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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