A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3526300



Internal ID22395680
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:28639104..28639377hg38UCSC Ensembl
chr1:28965616..28965889hg19UCSC Ensembl
Cytoband1p35.3
Allele length
AssemblyAllele length
hg38274
hg19274
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14359115, nssv14359114, nssv14359117, nssv14359116
SamplesNA19238, HG00731, HG00732, HG00513
Known GenesTAF12
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3526300
Frequency
Sample Size9
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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