A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5879223



Internal ID22654192
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:28460864..28462585hg38UCSC Ensembl
chr1:28787375..28789096hg19UCSC Ensembl
Cytoband1p35.3
Allele length
AssemblyAllele length
hg381722
hg191722
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17364935
Samples
Known GenesPHACTR4
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5879223
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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