A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5981781



Internal ID21891124
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:179638157..179638924hg38UCSC Ensembl
chr1:179607292..179608059hg19UCSC Ensembl
Cytoband1q25.2
Allele length
AssemblyAllele length
hg38768
hg19768
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17534593
Samples
Known GenesTDRD5
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5981781
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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