A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5476028



Internal ID253650
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:29814173..29817630hg38UCSC Ensembl
chr8:29671689..29675146hg19UCSC Ensembl
Cytoband8p12
Allele length
AssemblyAllele length
hg383458
hg193458
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17009254
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5476028
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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