A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17547096



Internal ID21871451
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:42089532..42090471hg38UCSC Ensembl
chr5:42089634..42090573hg19UCSC Ensembl
Cytoband5p13.1
Allele length
AssemblyAllele length
hg38940
hg19940
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5999731
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17547096
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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