A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5643450



Internal ID21591755
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:11354385..11354385hg38UCSC Ensembl
chr10:11396384..11396384hg19UCSC Ensembl
Cytoband10p14
Allele length
AssemblyAllele length
hg38331
hg19331
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17068341
SamplesHG02818
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5643450
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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