A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5561895



Internal ID334862
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:23119138..23219486hg38UCSC Ensembl
chr8:22976651..23076999hg19UCSC Ensembl
Cytoband8p21.3
Allele length
AssemblyAllele length
hg38100349
hg19100349
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17010316
Samples
Known GenesTNFRSF10A, TNFRSF10D
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5561895
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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