A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5578790



Internal ID21527262
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 StatusM
Merged Variants
Supporting Variantsnssv17060899
SamplesNA19238
Known GenesTNFRSF1B
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5578790
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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