A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17550832



Internal ID21875187
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:118022909..118044864hg38UCSC Ensembl
chr5:117358604..117380559hg19UCSC Ensembl
Cytoband5q23.1
Allele length
AssemblyAllele length
hg3821956
hg1921956
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6016874
Supporting Variants
Samples
Known GenesLOC102467224
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17550832
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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