A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5574372



Internal ID21522787
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:84287310..84287365hg38UCSC Ensembl
chr8:85199545..85199600hg19UCSC Ensembl
Cytoband8q21.2
Allele length
AssemblyAllele length
hg3856
hg1956
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17155447
SamplesHG00731
Known GenesRALYL
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5574372
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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