A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3225417



Internal ID22368552
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:128356700..128356850hg38UCSC Ensembl
chr9:131118979..131119129hg19UCSC Ensembl
Cytoband9q34.11
Allele length
AssemblyAllele length
hg38151
hg19151
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14348432, nssv14348431
SamplesNA19239, HG00513
Known GenesSLC27A4
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3225417
Frequency
Sample Size9
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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