A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5660952



Internal ID21609257
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:77490110..77490110hg38UCSC Ensembl
chr14:77956453..77956453hg19UCSC Ensembl
Cytoband14q24.3
Allele length
AssemblyAllele length
hg38134
hg19134
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17091063
SamplesHG03371
Known GenesISM2
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5660952
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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