A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3188284



Internal ID22340166
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:147865815..147872175hg38UCSC Ensembl
chr5:147245378..147251738hg19UCSC Ensembl
Cytoband5q32
Allele length
AssemblyAllele length
hg386361
hg196361
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14323609, nssv14323610, nssv14323608
SamplesHG00512, HG00513, HG00514
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Commentscomplex variant
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3188284
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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