A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5580839



Internal ID21529333
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:78694381..78694455hg38UCSC Ensembl
chr1:79160066..79160140hg19UCSC Ensembl
Cytoband1p31.1
Allele length
AssemblyAllele length
hg3875
hg1975
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17066115
SamplesHG03371
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5580839
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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