A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5907239



Internal ID22682444
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:15595205..15595310hg38UCSC Ensembl
chr5:15595314..15595419hg19UCSC Ensembl
Cytoband5p15.1
Allele length
AssemblyAllele length
hg38106
hg19106
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17414112
Samples
Known GenesFBXL7
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5907239
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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