A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5954883



Internal ID22730109
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:35633915..35634549hg38UCSC Ensembl
chr20:34221837..34222471hg19UCSC Ensembl
Cytoband20q11.22
Allele length
AssemblyAllele length
hg38635
hg19635
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17398395
Samples
Known GenesCPNE1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5954883
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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