A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6013359



Internal ID21922702
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:117884013..118730699hg38UCSC Ensembl
chr5:117219708..118066394hg19UCSC Ensembl
Cytoband5q23.1
Allele length
AssemblyAllele length
hg38846687
hg19846687
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17556932
Samples
Known GenesLOC100505811, LOC101927280, LOC102467224, LOC102467225
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6013359
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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