A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv876755



Internal ID6283766
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:46899516..47052937hg19UCSC Ensembl
Outerchr3:46895109..47061183hg19UCSC Ensembl
Innerchr3:46874520..47027941hg18UCSC Ensembl
Outerchr3:46870113..47036187hg18UCSC Ensembl
Cytoband3p21.31
Allele length
AssemblyAllele length
hg19n/a
hg18n/a
Variant TypeCNV Loss
Copy Number
Allele State
Allele Origin
Probe Count
Merged StatusS
Merged Variants
Supporting Variantsnssv1546526
SamplesMS17208
Known GenesCCDC12, MYL3, NBEAL2, NRADDP, PTH1R, SETD2
Method
Analysis
PlatformIllumina HumanHap 610 Quad + Illumina HumanHap 1MduoV3
Comments
ReferenceXu_et_al_2011
Pubmed ID21882294
Accession Number(s)nsv876755
Frequency
Sample Size6533
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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