A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5984061



Internal ID21893404
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:36632554..36632613hg38UCSC Ensembl
chr1:37098155..37098214hg19UCSC Ensembl
Cytoband1p34.3
Allele length
AssemblyAllele length
hg3860
hg1960
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17522857
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5984061
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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