A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5980760



Internal ID21890103
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:114804430..114804569hg38UCSC Ensembl
chr1:115347051..115347190hg19UCSC Ensembl
Cytoband1p13.2
Allele length
AssemblyAllele length
hg38140
hg19140
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17521423
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5980760
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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