A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4432260



Internal ID21394262
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:77616659..77618658hg38UCSC Ensembl
chr15:77909001..77911000hg19UCSC Ensembl
Cytoband15q24.3
Allele length
AssemblyAllele length
hg382000
hg192000
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15746839, nssv15753656
SamplesNB08, SMI041
Known GenesLINGO1
MethodSequencing
Analysis
Platform
Comments
ReferenceDeng_et_al_2019
Pubmed ID31718558
Accession Number(s)nsv4432260
Frequency
Sample Size15
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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