A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5980699



Internal ID21890042
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:102761082..102772137hg38UCSC Ensembl
chr1:103226638..103237693hg19UCSC Ensembl
Cytoband1p21.1
Allele length
AssemblyAllele length
hg3811056
hg1911056
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17518186
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5980699
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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