A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17549765



Internal ID21874120
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:30009341..30209423hg38UCSC Ensembl
chr5:30009448..30209530hg19UCSC Ensembl
Cytoband5p13.3
Allele length
AssemblyAllele length
hg38200083
hg19200083
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5999586
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17549765
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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