A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5905432



Internal ID22680619
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:157861856..157876239hg38UCSC Ensembl
chr5:157288864..157303247hg19UCSC Ensembl
Cytoband5q33.3
Allele length
AssemblyAllele length
hg3814384
hg1914384
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17419191
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5905432
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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