A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5902729



Internal ID22677890
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:15603540..15606516hg38UCSC Ensembl
chr5:15603649..15606625hg19UCSC Ensembl
Cytoband5p15.1
Allele length
AssemblyAllele length
hg382977
hg192977
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1650n209
Supporting Variantsnssv17425907
Samples
Known GenesFBXL7
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5902729
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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