A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5558012



Internal ID331089
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:167920726..167920830hg38UCSC Ensembl
chr1:167889964..167890068hg19UCSC Ensembl
Cytoband1q24.2
Allele length
AssemblyAllele length
hg38105
hg19105
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16892098
Samples
Known GenesMPC2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5558012
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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