A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5887515



Internal ID22662507
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:28286641..28289920hg38UCSC Ensembl
chr1:28613152..28616431hg19UCSC Ensembl
Cytoband1p35.3
Allele length
AssemblyAllele length
hg383280
hg193280
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17363951
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5887515
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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