A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5905907



Internal ID22681100
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:108212084..108213924hg38UCSC Ensembl
chr5:107547785..107549625hg19UCSC Ensembl
Cytoband5q21.3
Allele length
AssemblyAllele length
hg381841
hg191841
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17426607
Samples
Known GenesFBXL17
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5905907
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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