A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv877132



Internal ID6284143
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:87257423..87351380hg19UCSC Ensembl
Outerchr3:87241497..87357589hg19UCSC Ensembl
Innerchr3:87340113..87434070hg18UCSC Ensembl
Outerchr3:87324187..87440279hg18UCSC Ensembl
Cytoband3p11.2
Allele length
AssemblyAllele length
hg19n/a
hg18n/a
Variant TypeCNV Loss
Copy Number
Allele State
Allele Origin
Probe Count
Merged StatusS
Merged Variants
Supporting Variantsnssv1568108
SamplesIS31205
Known GenesCHMP2B, MIR4795, POU1F1
Method
Analysis
PlatformIllumina HumanHap 610 Quad + Illumina HumanHap 1MduoV3
Comments
ReferenceXu_et_al_2011
Pubmed ID21882294
Accession Number(s)nsv877132
Frequency
Sample Size6533
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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