A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5939856



Internal ID22715255
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:3913400..3913844hg38UCSC Ensembl
chr20:3894047..3894491hg19UCSC Ensembl
Cytoband20p13
Allele length
AssemblyAllele length
hg38445
hg19445
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17397249
Samples
Known GenesPANK2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5939856
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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