A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3558259



Internal ID22427062
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:53826782..53829669hg38UCSC Ensembl
chr5:53122612..53125499hg19UCSC Ensembl
Cytoband5q11.2
Allele length
AssemblyAllele length
hg382888
hg192888
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14321545, nssv14321544, nssv14321546, nssv14321542, nssv14321543
SamplesNA19239, HG00731, HG00732, NA19240, HG00733
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3558259
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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