A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5898689



Internal ID22673808
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 StatusM
Merged Variants
Supporting Variantsnssv17419633
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5898689
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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