A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6569429



Internal ID20942500
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:26042018..26042971hg38UCSC Ensembl
chr4:26043640..26044593hg19UCSC Ensembl
Cytoband4p15.2
Allele length
AssemblyAllele length
hg38954
hg19954
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18264963
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6569429
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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