A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5562412



Internal ID335367
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:43326358..43343439hg38UCSC Ensembl
chr5:43326460..43343541hg19UCSC Ensembl
Cytoband5p12
Allele length
AssemblyAllele length
hg3817082
hg1917082
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16967714
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5562412
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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