A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17547611



Internal ID21871966
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:6013641..6022361hg38UCSC Ensembl
chr5:6013754..6022474hg19UCSC Ensembl
Cytoband5p15.32
Allele length
AssemblyAllele length
hg388721
hg198721
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6000213
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17547611
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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