A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5580645



Internal ID21529137
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:77752521..77752856hg38UCSC Ensembl
chr5:77048345..77048680hg19UCSC Ensembl
Cytoband5q14.1
Allele length
AssemblyAllele length
hg38336
hg19336
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17155748
SamplesHG00731
Known GenesTBCA
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5580645
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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