A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18264963



Internal ID20832003
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 StatusS
Merged Variantsnsv6569429
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18264963
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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