A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17413452



Internal ID22471322
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:73869617..73871752hg38UCSC Ensembl
chr4:74735334..74737469hg19UCSC Ensembl
Cytoband4q13.3
Allele length
AssemblyAllele length
hg382136
hg192136
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5890995
Supporting Variants
Samples
Known GenesCXCL1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17413452
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.001


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