A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv882902



Internal ID6289913
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:131665378..131694360hg19UCSC Ensembl
Outerchr5:131663062..131707095hg19UCSC Ensembl
Innerchr5:131693277..131722259hg18UCSC Ensembl
Outerchr5:131690961..131734994hg18UCSC Ensembl
Cytoband5q31.1
Allele length
AssemblyAllele length
hg19n/a
hg18n/a
Variant TypeCNV Loss
Copy Number
Allele State
Allele Origin
Probe Count
Merged StatusM
Merged Variants
Supporting Variantsnssv1572207, nssv1540226
SamplesMS14752, IS32891
Known GenesLOC553103, MIR3936, SLC22A4, SLC22A5
Method
Analysis
PlatformIllumina HumanHap 610 Quad + Illumina HumanHap 1MduoV3
Comments
ReferenceXu_et_al_2011
Pubmed ID21882294
Accession Number(s)nsv882902
Frequency
Sample Size6533
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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