A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17060899



Internal ID21491850
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:12174139..12174195hg38UCSC Ensembl
chr1:12234196..12234252hg19UCSC Ensembl
Cytoband1p36.22
Allele length
AssemblyAllele length
hg3857
hg1957
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5578790
Supporting Variants
SamplesNA19238
Known GenesTNFRSF1B
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17060899
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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