A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17594099



Internal ID21786142
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:126425132..126425132hg38UCSC Ensembl
chr10:128113701..128113701hg19UCSC Ensembl
Cytoband10q26.2
Allele length
AssemblyAllele length
hg386000
hg196000
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6093406
Supporting Variants
Samples
Known GenesC10orf90
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17594099
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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