A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5982213



Internal ID21891556
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:182741223..182741352hg38UCSC Ensembl
chr1:182710358..182710487hg19UCSC Ensembl
Cytoband1q25.3
Allele length
AssemblyAllele length
hg38130
hg19130
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17537331
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5982213
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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