A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5983301



Internal ID21892644
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:244348581..244348847hg38UCSC Ensembl
chr1:244511883..244512149hg19UCSC Ensembl
Cytoband1q44
Allele length
AssemblyAllele length
hg38267
hg19267
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17522208
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5983301
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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