A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17417361



Internal ID22475231
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:163174606..163264058hg38UCSC Ensembl
chr3:162892394..162981846hg19UCSC Ensembl
Cytoband3q26.1
Allele length
AssemblyAllele length
hg3889453
hg1989453
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5896587
Supporting Variants
Samples
Known GenesCT64
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17417361
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.001


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