A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17417469



Internal ID22475339
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:167171644..167183564hg38UCSC Ensembl
chr5:166598649..166610569hg19UCSC Ensembl
Cytoband5q34
Allele length
AssemblyAllele length
hg3811921
hg1911921
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5898673
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17417469
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.001


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