A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6145880



Internal ID345085
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:41343894..41344020hg38UCSC Ensembl
chr19:41849799..41849925hg19UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg38127
hg19127
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17723489
Samples
Known GenesTGFB1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv6145880
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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