A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5555778



Internal ID328928
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:101205964..101206621hg38UCSC Ensembl
chr10:102965721..102966378hg19UCSC Ensembl
Cytoband10q24.31
Allele length
AssemblyAllele length
hg38658
hg19658
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17039451
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5555778
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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