A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17531294



Internal ID21855650
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:114383108..114384420hg38UCSC Ensembl
chr1:114925730..114927042hg19UCSC Ensembl
Cytoband1p13.2
Allele length
AssemblyAllele length
hg381313
hg191313
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5980922
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17531294
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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