A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3559215



Internal ID22428019
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:122836537..122836537hg38UCSC Ensembl
chr11:122707245..122707245hg19UCSC Ensembl
Cytoband11q24.1
Allele length
AssemblyAllele length
hg3877
hg1977
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14361430, nssv14361431, nssv14361432
SamplesHG00512, NA19238, HG00513
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3559215
Frequency
Sample Size9
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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