A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6559135



Internal ID20932206
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:111805508..111806386hg38UCSC Ensembl
chr3:111524355..111525233hg19UCSC Ensembl
Cytoband3q13.2
Allele length
AssemblyAllele length
hg38879
hg19879
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18259196
Samples
Known GenesPHLDB2, PLCXD2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6559135
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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