A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5868096



Internal ID22643031
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:211499037..211499117hg38UCSC Ensembl
chr1:211672379..211672459hg19UCSC Ensembl
Cytoband1q32.3
Allele length
AssemblyAllele length
hg3881
hg1981
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17355960
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5868096
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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