A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5590007



Internal ID21538575
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:34129740..34129815hg38UCSC Ensembl
chr20:32717546..32717621hg19UCSC Ensembl
Cytoband20q11.22
Allele length
AssemblyAllele length
hg3876
hg1976
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17116539
SamplesHG00732
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5590007
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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