A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3559108



Internal ID22427911
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:128186729..128186729hg38UCSC Ensembl
chr11:128056624..128056624hg19UCSC Ensembl
Cytoband11q24.3
Allele length
AssemblyAllele length
hg3864
hg1964
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14362202, nssv14362201
SamplesHG00732, HG00733
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3559108
Frequency
Sample Size9
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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