A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5485341



Internal ID262732
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:106268001..106268102hg38UCSC Ensembl
chr7:105908447..105908548hg19UCSC Ensembl
Cytoband7q22.3
Allele length
AssemblyAllele length
hg38102
hg19102
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17000899
Samples
Known GenesNAMPT
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5485341
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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