A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv911783



Internal ID6273710
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:42583493..42621482hg19UCSC Ensembl
Outerchr19:42575462..42624662hg19UCSC Ensembl
Innerchr19:47275333..47313322hg18UCSC Ensembl
Outerchr19:47267302..47316502hg18UCSC 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 Variantsnssv1510353
SamplesSP54956
Known GenesPOU2F2, ZNF574
Method
Analysis
PlatformIllumina HumanHap 610 Quad + Illumina HumanHap 1MduoV3
Comments
ReferenceXu_et_al_2011
Pubmed ID21882294
Accession Number(s)nsv911783
Frequency
Sample Size6533
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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