A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5880589



Internal ID22655559
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:109071684..109072275hg38UCSC Ensembl
chr1:109614306..109614897hg19UCSC Ensembl
Cytoband1p13.3
Allele length
AssemblyAllele length
hg38592
hg19592
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17352378
Samples
Known GenesTAF13
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5880589
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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