A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5981015



Internal ID21890358
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:12090096..12090192hg38UCSC Ensembl
chr1:12150153..12150249hg19UCSC Ensembl
Cytoband1p36.22
Allele length
AssemblyAllele length
hg3897
hg1997
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17534788
Samples
Known GenesTNFRSF8
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5981015
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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