A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5601402



Internal ID21550049
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:16059656..16059749hg38UCSC Ensembl
chr20:16040301..16040394hg19UCSC Ensembl
Cytoband20p12.1
Allele length
AssemblyAllele length
hg3894
hg1994
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17115852
SamplesNA12878
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5601402
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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