A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5984888



Internal ID21894231
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:62228103..62233287hg38UCSC Ensembl
chr1:62693775..62698959hg19UCSC Ensembl
Cytoband1p31.3
Allele length
AssemblyAllele length
hg385185
hg195185
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17518029
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5984888
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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