A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5589963



Internal ID21538531
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:25771068..25771205hg38UCSC Ensembl
chr20:25751704..25751841hg19UCSC Ensembl
Cytoband20p11.1
Allele length
AssemblyAllele length
hg38138
hg19138
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17115946
SamplesHG03683
Known GenesFAM182B
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5589963
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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