A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5556352



Internal ID329491
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:160408730..160409794hg38UCSC Ensembl
chr1:160378520..160379584hg19UCSC Ensembl
Cytoband1q23.2
Allele length
AssemblyAllele length
hg381065
hg191065
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16891075
Samples
Known GenesVANGL2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5556352
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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