A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5992079



Internal ID21901422
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:150160276..150160588hg38UCSC Ensembl
chr3:149878063..149878375hg19UCSC Ensembl
Cytoband3q25.1
Allele length
AssemblyAllele length
hg38313
hg19313
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17543095
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5992079
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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