A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv877136



Internal ID6284147
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:87307547..87363580hg19UCSC Ensembl
Outerchr3:87301395..87371282hg19UCSC Ensembl
Innerchr3:87390237..87446270hg18UCSC Ensembl
Outerchr3:87384085..87453972hg18UCSC Ensembl
Cytoband3p11.2
Allele length
AssemblyAllele length
hg19n/a
hg18n/a
Variant TypeCNV Gain
Copy Number
Allele State
Allele Origin
Probe Count
Merged StatusS
Merged Variants
Supporting Variantsnssv1540605
SamplesMS14933
Known GenesCHMP2B, POU1F1
Method
Analysis
PlatformIllumina HumanHap 610 Quad + Illumina HumanHap 1MduoV3
Comments
ReferenceXu_et_al_2011
Pubmed ID21882294
Accession Number(s)nsv877136
Frequency
Sample Size6533
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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