A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5475191



Internal ID252837
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:14773093..15804187hg38UCSC Ensembl
chr8:14630602..15661696hg19UCSC Ensembl
Cytoband8p22
Allele length
AssemblyAllele length
hg381031095
hg191031095
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17007495
Samples
Known GenesMIR383, SGCZ, TUSC3
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5475191
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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