A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5982989



Internal ID21892332
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:241533092..241533234hg38UCSC Ensembl
chr1:241696392..241696534hg19UCSC Ensembl
Cytoband1q43
Allele length
AssemblyAllele length
hg38143
hg19143
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17523896
Samples
Known GenesKMO
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5982989
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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