A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6138654



Internal ID337838
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:159042587..159048390hg38UCSC Ensembl
chr1:159012377..159018180hg19UCSC Ensembl
Cytoband1q23.1
Allele length
AssemblyAllele length
hg385804
hg195804
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16891437
Samples
Known GenesIFI16
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv6138654
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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