A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5586370



Internal ID21534923
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:7718403..7722232hg38UCSC Ensembl
chr20:7699050..7702879hg19UCSC Ensembl
Cytoband20p12.3
Allele length
AssemblyAllele length
hg383830
hg193830
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17118982
SamplesNA24385
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5586370
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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