A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17527169



Internal ID21851526
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:144826063..144826703hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg38641
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5981096
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17527169
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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