A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17523874



Internal ID21848233
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:173789779..173789779hg38UCSC Ensembl
chr1:173758917..173758917hg19UCSC Ensembl
Cytoband1q25.1
Allele length
AssemblyAllele length
hg38595
hg19595
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6045073
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17523874
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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