A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5981929



Internal ID21891272
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:168242877..168245242hg38UCSC Ensembl
chr1:168212115..168214480hg19UCSC Ensembl
Cytoband1q24.2
Allele length
AssemblyAllele length
hg382366
hg192366
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17523178
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5981929
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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