A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6568373



Internal ID20941444
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:151802104..151802699hg38UCSC Ensembl
chr5:151181665..151182260hg19UCSC Ensembl
Cytoband5q33.1
Allele length
AssemblyAllele length
hg38596
hg19596
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18268725
Samples
Known GenesG3BP1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6568373
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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