A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv882898



Internal ID6289909
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:131656517..131765206hg19UCSC Ensembl
Outerchr5:131652529..131770805hg19UCSC Ensembl
Innerchr5:131684416..131793105hg18UCSC Ensembl
Outerchr5:131680428..131798704hg18UCSC 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 Variantsnssv1579175
SamplesIS35028
Known GenesC5orf56, LOC553103, MIR3936, SLC22A4, SLC22A5
Method
Analysis
PlatformIllumina HumanHap 610 Quad + Illumina HumanHap 1MduoV3
Comments
ReferenceXu_et_al_2011
Pubmed ID21882294
Accession Number(s)nsv882898
Frequency
Sample Size6533
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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