A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5992312



Internal ID21901655
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:154378944..154379270hg38UCSC Ensembl
chr3:154096733..154097059hg19UCSC Ensembl
Cytoband3q25.2
Allele length
AssemblyAllele length
hg38327
hg19327
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17552779
Samples
Known GenesGPR149
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5992312
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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