A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5580935



Internal ID21529430
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:90001606..90001666hg38UCSC Ensembl
chr8:91013834..91013894hg19UCSC Ensembl
Cytoband8q21.3
Allele length
AssemblyAllele length
hg3861
hg1961
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17140072
SamplesNA20847
Known GenesDECR1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5580935
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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