A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5433250



Internal ID211973
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:67767775..67767826hg38UCSC Ensembl
chr15:68060113..68060164hg19UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg38280
hg19280
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17702940
Samples
Known GenesMAP2K5
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5433250
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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