A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv527279



Internal ID6021379
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:86845934..87863280hg19UCSC Ensembl
Innerchr3:86928624..87945970hg18UCSC Ensembl
Innerchr3:86928624..87945970hg17UCSC Ensembl
Cytoband3p11.2
Allele length
AssemblyAllele length
hg19n/a
hg18n/a
hg17n/a
Variant TypeCNV Gain
Copy Number
Allele State
Allele OriginNot tested
Probe Count
Merged StatusS
Merged Variants
Supporting Variantsnssv703691
Samples
Known GenesCHMP2B, MIR4795, POU1F1, VGLL3
Method
AnalysisCNV regions located outside of or spanning over several merged-level regions determined by the submitter
PlatformIllumina HumanHap550 Genotyping BeadChip v3
Comments
ReferenceShaikh et al 2009
Pubmed ID19592680
Accession Number(s)nsv527279
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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