A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5591456



Internal ID21540031
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:56672750..56679541hg38UCSC Ensembl
chr20:55247806..55254597hg19UCSC Ensembl
Cytoband20q13.31
Allele length
AssemblyAllele length
hg386792
hg196792
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17117017
SamplesHG00732
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5591456
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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