A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17552779



Internal ID21877134
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 StatusS
Merged Variantsnsv5992312
Supporting Variants
Samples
Known GenesGPR149
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17552779
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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