A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5991690



Internal ID21901033
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:155526403..155526468hg38UCSC Ensembl
chr3:155244192..155244257hg19UCSC Ensembl
Cytoband3q25.31
Allele length
AssemblyAllele length
hg3866
hg1966
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17554236
Samples
Known GenesPLCH1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5991690
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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