A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5981624



Internal ID21890967
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:152303179..152312927hg38UCSC Ensembl
chr1:152275655..152285403hg19UCSC Ensembl
Cytoband1q21.3
Allele length
AssemblyAllele length
hg389749
hg199749
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17524101
Samples
Known GenesFLG
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5981624
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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