A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5485575



Internal ID262963
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:10218282..10236619hg38UCSC Ensembl
chr8:10075792..10094129hg19UCSC Ensembl
Cytoband8p23.1
Allele length
AssemblyAllele length
hg3818338
hg1918338
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17007361
Samples
Known GenesMSRA
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5485575
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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