A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17402661



Internal ID22460531
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:116818301..116818366hg38UCSC Ensembl
chr3:116537148..116537213hg19UCSC Ensembl
Cytoband3q13.31
Allele length
AssemblyAllele length
hg3866
hg1966
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5900156
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17402661
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.001


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