A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5587639



Internal ID21536197
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:63919438..63919661hg38UCSC Ensembl
chr20:62550791..62551014hg19UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg38224
hg19224
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17117781
SamplesHG02011
Known GenesDNAJC5, MIR941-1, MIR941-3, MIR941-4
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5587639
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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