A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5559243



Internal ID332283
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:43008707..43015506hg38UCSC Ensembl
chr4:43010724..43017523hg19UCSC Ensembl
Cytoband4p13
Allele length
AssemblyAllele length
hg386800
hg196800
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16949698
Samples
Known GenesGRXCR1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5559243
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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