A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5984823



Internal ID21894166
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:733251..914825hg38UCSC Ensembl
chr1:668631..850205hg19UCSC Ensembl
Cytoband1p36.33
Allele length
AssemblyAllele length
hg38181575
hg19181575
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17532927
Samples
Known GenesFAM41C, FAM87B, LINC00115, LINC01128, LOC100288069
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5984823
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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