A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6144268



Internal ID343472
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:86980066..86986100hg38UCSC Ensembl
chr15:87523297..87529331hg19UCSC Ensembl
Cytoband15q25.3
Allele length
AssemblyAllele length
hg386035
hg196035
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv178n206
Supporting Variantsnssv17705446
Samples
Known GenesAGBL1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv6144268
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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