A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv881045



Internal ID6288056
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:35857177..35860637hg19UCSC Ensembl
Outerchr5:35856575..35861068hg19UCSC Ensembl
Innerchr5:35892934..35896394hg18UCSC Ensembl
Outerchr5:35892332..35896825hg18UCSC Ensembl
Cytoband5p13.2
Allele length
AssemblyAllele length
hg19n/a
hg18n/a
Variant TypeCNV Loss
Copy Number
Allele State
Allele Origin
Probe Count
Merged StatusM
Merged Variants
Supporting Variantsnssv1513831, nssv1502692
SamplesSP55851, SP51339
Known GenesIL7R
Method
Analysis
PlatformIllumina HumanHap 610 Quad + Illumina HumanHap 1MduoV3
Comments
ReferenceXu_et_al_2011
Pubmed ID21882294
Accession Number(s)nsv881045
Frequency
Sample Size6533
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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