A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17592218



Internal ID21784261
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:114083952..114083952hg38UCSC Ensembl
chr10:115843711..115843711hg19UCSC Ensembl
Cytoband10q25.3
Allele length
AssemblyAllele length
hg3880
hg1980
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6082268
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17592218
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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