A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv911593



Internal ID6273520
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:33726375..33791127hg19UCSC Ensembl
Outerchr19:33723705..33802542hg19UCSC Ensembl
Innerchr19:38418215..38482967hg18UCSC Ensembl
Outerchr19:38415545..38494382hg18UCSC 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 Variantsnssv1574647
SamplesIS33601
Known GenesCEBPA, LOC80054
Method
Analysis
PlatformIllumina HumanHap 610 Quad + Illumina HumanHap 1MduoV3
Comments
ReferenceXu_et_al_2011
Pubmed ID21882294
Accession Number(s)nsv911593
Frequency
Sample Size6533
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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