A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv877387



Internal ID6284398
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:121889088..121918491hg19UCSC Ensembl
Outerchr3:121873433..121934161hg19UCSC Ensembl
Innerchr3:123371778..123401181hg18UCSC Ensembl
Outerchr3:123356123..123416851hg18UCSC Ensembl
Cytoband3q13.33
Allele length
AssemblyAllele length
hg19n/a
hg18n/a
Variant TypeCNV Loss
Copy Number
Allele State
Allele Origin
Probe Count
Merged StatusS
Merged Variants
Supporting Variantsnssv1585817
SamplesIS37646
Known GenesCASR
Method
Analysis
PlatformIllumina HumanHap 610 Quad + Illumina HumanHap 1MduoV3
Comments
ReferenceXu_et_al_2011
Pubmed ID21882294
Accession Number(s)nsv877387
Frequency
Sample Size6533
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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