A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17533701



Internal ID21858057
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:114828099..114836333hg38UCSC Ensembl
chr1:115370720..115378954hg19UCSC Ensembl
Cytoband1p13.2
Allele length
AssemblyAllele length
hg388235
hg198235
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5980924
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17533701
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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