A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17585923



Internal ID21777966
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:125228053..125228053hg38UCSC Ensembl
chr10:126916622..126916622hg19UCSC Ensembl
Cytoband10q26.13
Allele length
AssemblyAllele length
hg38118
hg19118
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6097931
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17585923
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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