A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6569914



Internal ID20942985
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:169310919..169312313hg38UCSC Ensembl
chr4:170232070..170233464hg19UCSC Ensembl
Cytoband4q33
Allele length
AssemblyAllele length
hg381395
hg191395
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18264381
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6569914
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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