A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5491375



Internal ID268614
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:38721182..38730340hg38UCSC Ensembl
chr8:38578700..38587858hg19UCSC Ensembl
Cytoband8p11.22
Allele length
AssemblyAllele length
hg389159
hg199159
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17010708
Samples
Known GenesTACC1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5491375
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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