A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5953897



Internal ID22729166
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:42705821..42711336hg38UCSC Ensembl
chr21:44125931..44131446hg19UCSC Ensembl
Cytoband21q22.3
Allele length
AssemblyAllele length
hg385516
hg195516
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17405956
Samples
Known GenesPDE9A
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5953897
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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