A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5478081



Internal ID255645
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:144738804..144760804hg38UCSC Ensembl
chr7:144435897..144457897hg19UCSC Ensembl
Cytoband7q35
Allele length
AssemblyAllele length
hg3822001
hg1922001
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17004698
Samples
Known GenesTPK1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5478081
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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