A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5603711



Internal ID21552376
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:25767862..25770261hg38UCSC Ensembl
chr20:25748498..25750897hg19UCSC Ensembl
Cytoband20p11.1
Allele length
AssemblyAllele length
hg382400
hg192400
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17115944
SamplesHG01596
Known GenesFAM182B
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5603711
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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