A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6143802



Internal ID343003
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:105776900..105782000hg38UCSC Ensembl
chr12:106170678..106175778hg19UCSC Ensembl
Cytoband12q23.3
Allele length
AssemblyAllele length
hg385101
hg195101
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17690588
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv6143802
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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