A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17423758



Internal ID22481628
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:184318704..184318704hg38UCSC Ensembl
chr4:185239857..185239857hg19UCSC Ensembl
Cytoband4q35.1
Allele length
AssemblyAllele length
hg38168
hg19168
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5949149
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17423758
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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