A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17531568



Internal ID21855924
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:162611247..162614304hg38UCSC Ensembl
chr1:162581037..162584094hg19UCSC Ensembl
Cytoband1q23.3
Allele length
AssemblyAllele length
hg383058
hg193058
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5981903
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17531568
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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