A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5890565



Internal ID22665593
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:141062834..141062991hg38UCSC Ensembl
chr3:140781676..140781833hg19UCSC Ensembl
Cytoband3q23
Allele length
AssemblyAllele length
hg38158
hg19158
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17405565
Samples
Known GenesSPSB4
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5890565
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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