A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5655169



Internal ID21603474
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:67687390..67687390hg38UCSC Ensembl
chr15:67979728..67979728hg19UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg38319
hg19319
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17085615
SamplesHG03371
Known GenesMAP2K5
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5655169
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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