A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5984877



Internal ID21894220
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:610118..633818hg38UCSC Ensembl
chr1:545498..569198hg19UCSC Ensembl
Cytoband1p36.33
Allele length
AssemblyAllele length
hg3823701
hg1923701
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17522198
Samples
Known GenesMIR6723
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5984877
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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