A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5520284



Internal ID296615
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:59637257..59675367hg38UCSC Ensembl
chr15:59929456..59967566hg19UCSC Ensembl
Cytoband15q22.2
Allele length
AssemblyAllele length
hg3838111
hg1938111
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17700974
Samples
Known GenesBNIP2, GTF2A2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5520284
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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