A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6140083



Internal ID339275
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:113025000..113032787hg38UCSC Ensembl
chr3:112743847..112751634hg19UCSC Ensembl
Cytoband3q13.2
Allele length
AssemblyAllele length
hg387788
hg197788
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16938344
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv6140083
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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