A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5567150



Internal ID21515482
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:90684225..90685071hg38UCSC Ensembl
chr8:91696453..91697299hg19UCSC Ensembl
Cytoband8q21.3
Allele length
AssemblyAllele length
hg38847
hg19847
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17153783
SamplesHG03486
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5567150
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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