A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5526401



Internal ID302532
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:52032665..52033219hg38UCSC Ensembl
chr15:52324862..52325416hg19UCSC Ensembl
Cytoband15q21.2
Allele length
AssemblyAllele length
hg38555
hg19555
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17702734
Samples
Known GenesMAPK6
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5526401
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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