A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3526060



Internal ID22395440
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:10873400..10873552hg38UCSC Ensembl
chr3:10915085..10915237hg19UCSC Ensembl
Cytoband3p25.3
Allele length
AssemblyAllele length
hg38153
hg19153
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14304638, nssv14304637, nssv14304636
SamplesHG00512, HG00513, HG00514
Known GenesSLC6A11
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3526060
Frequency
Sample Size9
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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