A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5880719



Internal ID22655689
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:123470145..124011235hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg38541091
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv67n209
Supporting Variantsnssv17355296
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5880719
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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