A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17356937



Internal ID22582606
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 StatusS
Merged Variantsnsv5875337
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17356937
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequency1.00


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