A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17355302



Internal ID22580971
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:179255381..179275671hg38UCSC Ensembl
chr1:179224516..179244806hg19UCSC Ensembl
Cytoband1q25.2
Allele length
AssemblyAllele length
hg3820291
hg1920291
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5875854
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17355302
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.001


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