A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5879707



Internal ID22654679
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:28131782..28140655hg38UCSC Ensembl
chr1:28458293..28467166hg19UCSC Ensembl
Cytoband1p35.3
Allele length
AssemblyAllele length
hg388874
hg198874
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17354083
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5879707
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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