A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5981925



Internal ID21891268
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:167913652..167913730hg38UCSC Ensembl
chr1:167882890..167882968hg19UCSC Ensembl
Cytoband1q24.2
Allele length
AssemblyAllele length
hg3879
hg1979
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17528020
Samples
Known GenesADCY10
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5981925
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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