A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5601599



Internal ID21550248
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:15911464..15911556hg38UCSC Ensembl
chr20:15892109..15892201hg19UCSC Ensembl
Cytoband20p12.1
Allele length
AssemblyAllele length
hg3893
hg1993
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17115848
SamplesHG03065
Known GenesMACROD2
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5601599
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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