A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3527838



Internal ID22397225
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:92487987..92488593hg38UCSC Ensembl
chr15:93031217..93031823hg19UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg38607
hg19607
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14378511, nssv14380610
SamplesNA19239, NA19240
Known GenesC15orf32
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3527838
Frequency
Sample Size9
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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