A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5525830



Internal ID301978
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:101510809..101762551hg38UCSC Ensembl
chr15:102051012..102302754hg19UCSC Ensembl
Cytoband15q26.3
Allele length
AssemblyAllele length
hg38251743
hg19251743
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv185n206
Supporting Variantsnssv17703437
Samples
Known GenesTARSL2, TM2D3
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5525830
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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