A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17394137



Internal ID22452007
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:87451198..87451655hg38UCSC Ensembl
chr1:87916881..87917338hg19UCSC Ensembl
Cytoband1p22.3
Allele length
AssemblyAllele length
hg38458
hg19458
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5886096
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17394137
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.012


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