A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17587431



Internal ID21779474
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:103992656..103992656hg38UCSC Ensembl
chr10:105752414..105752414hg19UCSC Ensembl
Cytoband10q24.33
Allele length
AssemblyAllele length
hg38108
hg19108
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6089859
Supporting Variants
Samples
Known GenesSLK
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17587431
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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