A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5884978



Internal ID22659962
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:161290353..161290438hg38UCSC Ensembl
chr1:161260143..161260228hg19UCSC Ensembl
Cytoband1q23.3
Allele length
AssemblyAllele length
hg3886
hg1986
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17364470
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5884978
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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