A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17355980



Internal ID22581649
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:106478772..106495280hg38UCSC Ensembl
chr1:107021394..107037902hg19UCSC Ensembl
Cytoband1p21.1
Allele length
AssemblyAllele length
hg3816509
hg1916509
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5877922
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17355980
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.001


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