A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17360493



Internal ID22586162
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:182154263..182154389hg38UCSC Ensembl
chr1:182123398..182123524hg19UCSC Ensembl
Cytoband1q25.3
Allele length
AssemblyAllele length
hg38127
hg19127
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5869521
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17360493
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.009


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