A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5586471



Internal ID21535025
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:45744194..45758835hg38UCSC Ensembl
chr20:44372833..44387474hg19UCSC Ensembl
Cytoband20q13.12
Allele length
AssemblyAllele length
hg3814642
hg1914642
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17116949
SamplesHG00732
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5586471
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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