A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3226033



Internal ID22368978
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:86296413..86296476hg38UCSC Ensembl
chr15:86839644..86839707hg19UCSC Ensembl
Cytoband15q25.3
Allele length
AssemblyAllele length
hg3864
hg1964
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14379638
SamplesHG00731
Known GenesAGBL1
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3226033
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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