A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5583022



Internal ID21531541
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:129647236..129647285hg38UCSC Ensembl
chr8:130659482..130659531hg19UCSC Ensembl
Cytoband8q24.21
Allele length
AssemblyAllele length
hg3850
hg1950
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17149835
SamplesHG00731
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5583022
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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