A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5984913



Internal ID21894256
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:69585926..69617159hg38UCSC Ensembl
chr1:70051609..70082842hg19UCSC Ensembl
Cytoband1p31.1
Allele length
AssemblyAllele length
hg3831234
hg1931234
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17522518
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5984913
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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