A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv882890



Internal ID6289901
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:131626611..131681057hg19UCSC Ensembl
Outerchr5:131625169..131694360hg19UCSC Ensembl
Innerchr5:131654510..131708956hg18UCSC Ensembl
Outerchr5:131653068..131722259hg18UCSC Ensembl
Cytoband5q31.1
Allele length
AssemblyAllele length
hg19n/a
hg18n/a
Variant TypeCNV Loss
Copy Number
Allele State
Allele Origin
Probe Count
Merged StatusS
Merged Variants
Supporting Variantsnssv1539529
SamplesMS14359
Known GenesLOC553103, SLC22A4
Method
Analysis
PlatformIllumina HumanHap 610 Quad + Illumina HumanHap 1MduoV3
Comments
ReferenceXu_et_al_2011
Pubmed ID21882294
Accession Number(s)nsv882890
Frequency
Sample Size6533
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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