A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5542273



Internal ID316709
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:91689668..91689683hg38UCSC Ensembl
chr10:93449425..93449440hg19UCSC Ensembl
Cytoband10q23.32
Allele length
AssemblyAllele length
hg3868
hg1968
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17036918
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5542273
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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