A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5515396



Internal ID291876
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:15513000..15519111hg38UCSC Ensembl
chr17:15416314..15422425hg19UCSC Ensembl
Cytoband17p12
Allele length
AssemblyAllele length
hg386112
hg196112
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17711698
Samples
Known GenesTVP23C, TVP23C-CDRT4
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5515396
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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