A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5659287



Internal ID21607592
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:79438004..79438004hg38UCSC Ensembl
chr15:79730346..79730346hg19UCSC Ensembl
Cytoband15q25.1
Allele length
AssemblyAllele length
hg3875
hg1975
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17092816
SamplesNA19238
Known GenesKIAA1024
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5659287
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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