A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv911028



Internal ID6272955
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:10221414..10229850hg19UCSC Ensembl
Outerchr19:10219076..10230328hg19UCSC Ensembl
Innerchr19:10082414..10090850hg18UCSC Ensembl
Outerchr19:10080076..10091328hg18UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg19n/a
hg18n/a
Variant TypeCNV Loss
Copy Number
Allele State
Allele Origin
Probe Count
Merged StatusS
Merged Variants
Supporting Variantsnssv1511043
SamplesSP54988
Known GenesEIF3G, P2RY11, PPAN, PPAN-P2RY11, SNORD105B
Method
Analysis
PlatformIllumina HumanHap 610 Quad + Illumina HumanHap 1MduoV3
Comments
ReferenceXu_et_al_2011
Pubmed ID21882294
Accession Number(s)nsv911028
Frequency
Sample Size6533
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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