A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv876514



Internal ID6283525
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:8751984..9117788hg19UCSC Ensembl
Outerchr3:8749558..9119182hg19UCSC Ensembl
Innerchr3:8726984..9092788hg18UCSC Ensembl
Outerchr3:8724558..9094182hg18UCSC Ensembl
Cytoband3p25.3
Allele length
AssemblyAllele length
hg19n/a
hg18n/a
Variant TypeCNV Gain
Copy Number
Allele State
Allele Origin
Probe Count
Merged StatusS
Merged Variants
Supporting Variantsnssv1548538
SamplesMS17878
Known GenesCAV3, OXTR, RAD18, SRGAP3
Method
Analysis
PlatformIllumina HumanHap 610 Quad + Illumina HumanHap 1MduoV3
Comments
ReferenceXu_et_al_2011
Pubmed ID21882294
Accession Number(s)nsv876514
Frequency
Sample Size6533
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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