A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17419633



Internal ID22477503
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:178070457..178070530hg38UCSC Ensembl
chr5:177497458..177497531hg19UCSC Ensembl
Cytoband5q35.3
Allele length
AssemblyAllele length
hg3874
hg1974
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5898689
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17419633
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00


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