A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6139123



Internal ID338307
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:198163900..198180000hg38UCSC Ensembl
chr3:197890771..197906871hg19UCSC Ensembl
Cytoband3q29
Allele length
AssemblyAllele length
hg3816101
hg1916101
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16945279
Samples
Known GenesFAM157A
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv6139123
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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