A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5984029



Internal ID21893372
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:32974861..32975037hg38UCSC Ensembl
chr1:33440462..33440638hg19UCSC Ensembl
Cytoband1p35.1
Allele length
AssemblyAllele length
hg38177
hg19177
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17527967
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5984029
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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