A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv882904



Internal ID6289915
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:131668467..131675864hg19UCSC Ensembl
Outerchr5:131667548..131675981hg19UCSC Ensembl
Innerchr5:131696366..131703763hg18UCSC Ensembl
Outerchr5:131695447..131703880hg18UCSC 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 Variantsnssv1591255
SamplesIS38663
Known GenesLOC553103, SLC22A4
Method
Analysis
PlatformIllumina HumanHap 610 Quad + Illumina HumanHap 1MduoV3
Comments
ReferenceXu_et_al_2011
Pubmed ID21882294
Accession Number(s)nsv882904
Frequency
Sample Size6533
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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