A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5911745



Internal ID22686960
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:86692224..86692342hg38UCSC Ensembl
chr10:88451981..88452099hg19UCSC Ensembl
Cytoband10q23.2
Allele length
AssemblyAllele length
hg38119
hg19119
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17365888
Samples
Known GenesLDB3
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5911745
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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