A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5475766



Internal ID253399
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:50366669..50366934hg38UCSC Ensembl
chr8:51279229..51279494hg19UCSC Ensembl
Cytoband8q11.21
Allele length
AssemblyAllele length
hg38266
hg19266
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17011437
Samples
Known GenesSNTG1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5475766
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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