A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5574439



Internal ID21522854
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:15935240..15935381hg38UCSC Ensembl
chr5:15935349..15935490hg19UCSC Ensembl
Cytoband5p15.1
Allele length
AssemblyAllele length
hg38142
hg19142
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17126972
SamplesHG03732
Known GenesFBXL7
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5574439
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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