A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5585063



Internal ID21533607
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:61394349..61394469hg38UCSC Ensembl
chr20:59969405..59969525hg19UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg38121
hg19121
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17117563
SamplesHG03732
Known GenesCDH4
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5585063
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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