A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5984089



Internal ID21893432
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:39032109..39033134hg38UCSC Ensembl
chr1:39497781..39498806hg19UCSC Ensembl
Cytoband1p34.3
Allele length
AssemblyAllele length
hg381026
hg191026
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17525529
Samples
Known GenesNDUFS5
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5984089
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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