A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3528646



Internal ID22398035
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:73998970..73999168hg38UCSC Ensembl
chr11:73710015..73710213hg19UCSC Ensembl
Cytoband11q13.4
Allele length
AssemblyAllele length
hg38199
hg19199
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14357871
SamplesHG00733
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3528646
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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