A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5879128



Internal ID22654096
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:42705801..42711387hg38UCSC Ensembl
chr21:44125911..44131497hg19UCSC Ensembl
Cytoband21q22.3
Allele length
AssemblyAllele length
hg385587
hg195587
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17488905
Samples
Known GenesPDE9A
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5879128
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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