A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17580988



Internal ID21773031
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:59225143..59225143hg38UCSC Ensembl
chr10:60984903..60984903hg19UCSC Ensembl
Cytoband10q21.1
Allele length
AssemblyAllele length
hg38312
hg19312
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6080581
Supporting Variants
Samples
Known GenesPHYHIPL
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17580988
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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