A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5982342



Internal ID21891685
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:205528870..205530886hg38UCSC Ensembl
chr1:205497998..205500014hg19UCSC Ensembl
Cytoband1q32.1
Allele length
AssemblyAllele length
hg382017
hg192017
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17532832
Samples
Known GenesCDK18
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5982342
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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