A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3220983



Internal ID22365516
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:41400100..41400482hg38UCSC Ensembl
chr15:41692298..41692680hg19UCSC Ensembl
Cytoband15q15.1
Allele length
AssemblyAllele length
hg38383
hg19383
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14380142, nssv14375747
SamplesNA19238, HG00513
Known GenesNDUFAF1
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3220983
Frequency
Sample Size9
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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