A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3529892



Internal ID22399283
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:11283840..11284545hg38UCSC Ensembl
chr10:11325803..11326508hg19UCSC Ensembl
Cytoband10p14
Allele length
AssemblyAllele length
hg38706
hg19706
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14331178, nssv14331180, nssv14331177, nssv14331179
SamplesHG00512, HG00732, HG00733, HG00513
Known GenesCELF2
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3529892
Frequency
Sample Size9
Observed Gain4
Observed Loss0
Observed Complex0
Frequencyn/a


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