A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv911117



Internal ID6273044
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:14185226..14233348hg19UCSC Ensembl
Outerchr19:14181842..14233734hg19UCSC Ensembl
Innerchr19:14046226..14094348hg18UCSC Ensembl
Outerchr19:14042842..14094734hg18UCSC Ensembl
Cytoband19p13.12
Allele length
AssemblyAllele length
hg19n/a
hg18n/a
Variant TypeCNV Loss
Copy Number
Allele State
Allele Origin
Probe Count
Merged StatusS
Merged Variants
Supporting Variantsnssv1511590
SamplesSP55021
Known GenesASF1B, LOC113230, PRKACA, SAMD1
Method
Analysis
PlatformIllumina HumanHap 610 Quad + Illumina HumanHap 1MduoV3
Comments
ReferenceXu_et_al_2011
Pubmed ID21882294
Accession Number(s)nsv911117
Frequency
Sample Size6533
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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