A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv878400



Internal ID6285411
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:1762287..1816287hg19UCSC Ensembl
Outerchr4:1744252..1834422hg19UCSC Ensembl
Innerchr4:1732085..1786085hg18UCSC Ensembl
Outerchr4:1714050..1804220hg18UCSC Ensembl
Cytoband4p16.3
Allele length
AssemblyAllele length
hg19n/a
hg18n/a
Variant TypeCNV Loss
Copy Number
Allele State
Allele Origin
Probe Count
Merged StatusM
Merged Variants
Supporting Variantsnssv1544230, nssv1543417
SamplesMS16315, MS16153
Known GenesFGFR3, LETM1, TACC3
Method
Analysis
PlatformIllumina HumanHap 610 Quad + Illumina HumanHap 1MduoV3
Comments
ReferenceXu_et_al_2011
Pubmed ID21882294
Accession Number(s)nsv878400
Frequency
Sample Size6533
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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