A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5981683



Internal ID21891026
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:168584771..168584919hg38UCSC Ensembl
chr1:168554009..168554157hg19UCSC Ensembl
Cytoband1q24.2
Allele length
AssemblyAllele length
hg38149
hg19149
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17533551
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5981683
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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