A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17588021



Internal ID21780064
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:120733283..120734113hg38UCSC Ensembl
chr10:122492795..122493625hg19UCSC Ensembl
Cytoband10q26.12
Allele length
AssemblyAllele length
hg38831
hg19831
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6013825
Supporting Variants
Samples
Known GenesMIR5694
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17588021
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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