A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5875337



Internal ID22650294
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:123452648..123873774hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg38421127
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv67n209
Supporting Variantsnssv17356937
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5875337
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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