A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5906662



Internal ID22681864
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:15574881..15575276hg38UCSC Ensembl
chr5:15574990..15575385hg19UCSC Ensembl
Cytoband5p15.1
Allele length
AssemblyAllele length
hg38396
hg19396
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17428177
Samples
Known GenesFBXL7
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5906662
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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