A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv911769



Internal ID6273696
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:41814412..41839631hg19UCSC Ensembl
Outerchr19:41813676..41845801hg19UCSC Ensembl
Innerchr19:46506252..46531471hg18UCSC Ensembl
Outerchr19:46505516..46537641hg18UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg19n/a
hg18n/a
Variant TypeCNV Loss
Copy Number
Allele State
Allele Origin
Probe Count
Merged StatusS
Merged Variants
Supporting Variantsnssv1510351
SamplesSP54956
Known GenesCCDC97, HNRNPUL1, TGFB1
Method
Analysis
PlatformIllumina HumanHap 610 Quad + Illumina HumanHap 1MduoV3
Comments
ReferenceXu_et_al_2011
Pubmed ID21882294
Accession Number(s)nsv911769
Frequency
Sample Size6533
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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