A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5579781



Internal ID21528263
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:171096451..171096527hg38UCSC Ensembl
chr1:171065592..171065668hg19UCSC Ensembl
Cytoband1q24.3
Allele length
AssemblyAllele length
hg3877
hg1977
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17061329
SamplesHG00513
Known GenesFMO3
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5579781
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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