A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5984941



Internal ID21894284
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:7907166..7916913hg38UCSC Ensembl
chr1:7967226..7976973hg19UCSC Ensembl
Cytoband1p36.23
Allele length
AssemblyAllele length
hg389748
hg199748
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17519082
Samples
Known GenesTNFRSF9
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5984941
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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