A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17517600



Internal ID21841959
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:25178047..25178119hg38UCSC Ensembl
chr1:25504538..25504610hg19UCSC Ensembl
Cytoband1p36.11
Allele length
AssemblyAllele length
hg3873
hg1973
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5983686
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17517600
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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