A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv877133



Internal ID6284144
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:87284401..87308831hg19UCSC Ensembl
Outerchr3:87280088..87313147hg19UCSC Ensembl
Innerchr3:87367091..87391521hg18UCSC Ensembl
Outerchr3:87362778..87395837hg18UCSC Ensembl
Cytoband3p11.2
Allele length
AssemblyAllele length
hg19n/a
hg18n/a
Variant TypeCNV Loss
Copy Number
Allele State
Allele Origin
Probe Count
Merged StatusM
Merged Variants
Supporting Variantsnssv1500415, nssv1499234, nssv1515809
SamplesSP50073, SP50137, SP56289
Known GenesCHMP2B, POU1F1
Method
Analysis
PlatformIllumina HumanHap 610 Quad + Illumina HumanHap 1MduoV3
Comments
ReferenceXu_et_al_2011
Pubmed ID21882294
Accession Number(s)nsv877133
Frequency
Sample Size6533
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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