A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5563178



Internal ID336115
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:15742774..15760447hg38UCSC Ensembl
chr10:15784773..15802446hg19UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg3817674
hg1917674
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17032119
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5563178
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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