A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3559028



Internal ID22427833
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:130013972..130013972hg38UCSC Ensembl
chr10:131812236..131812236hg19UCSC Ensembl
Cytoband10q26.3
Allele length
AssemblyAllele length
hg3861
hg1961
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14356725, nssv14356726, nssv14356724, nssv14356723
SamplesHG00512, NA19238, NA19239, NA19240
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3559028
Frequency
Sample Size9
Observed Gain4
Observed Loss0
Observed Complex0
Frequencyn/a


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