A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5981570



Internal ID21890913
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:162664320..162680968hg38UCSC Ensembl
chr1:162634110..162650758hg19UCSC Ensembl
Cytoband1q23.3
Allele length
AssemblyAllele length
hg3816649
hg1916649
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17529401
Samples
Known GenesDDR2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5981570
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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