A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5436698



Internal ID215308
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:160944011..160949480hg38UCSC Ensembl
chr3:160661799..160667268hg19UCSC Ensembl
Cytoband3q25.33
Allele length
AssemblyAllele length
hg385470
hg195470
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16941980
Samples
Known GenesPPM1L
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5436698
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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