A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3230344



Internal ID22371899
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:48152993..48153044hg38UCSC Ensembl
chr15:48445190..48445241hg19UCSC Ensembl
Cytoband15q21.1
Allele length
AssemblyAllele length
hg3852
hg1952
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14387431
SamplesNA19239
Known GenesMYEF2
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3230344
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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