A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv911597



Internal ID6273524
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:33860858..33902809hg19UCSC Ensembl
Outerchr19:33852145..33906764hg19UCSC Ensembl
Innerchr19:38552698..38594649hg18UCSC Ensembl
Outerchr19:38543985..38598604hg18UCSC Ensembl
Cytoband19q13.11
Allele length
AssemblyAllele length
hg19n/a
hg18n/a
Variant TypeCNV Loss
Copy Number
Allele State
Allele Origin
Probe Count
Merged StatusS
Merged Variants
Supporting Variantsnssv1592450
SamplesIS39233
Known GenesCEBPG, PEPD
Method
Analysis
PlatformIllumina HumanHap 610 Quad + Illumina HumanHap 1MduoV3
Comments
ReferenceXu_et_al_2011
Pubmed ID21882294
Accession Number(s)nsv911597
Frequency
Sample Size6533
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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