A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv872590



Internal ID6279601
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:186580824..187492812hg19UCSC Ensembl
Outerchr1:186557453..187500338hg19UCSC Ensembl
Innerchr1:184847447..185759435hg18UCSC Ensembl
Outerchr1:184824076..185766961hg18UCSC Ensembl
Cytoband1q31.1
Allele length
AssemblyAllele length
hg19n/a
hg18n/a
Variant TypeCNV Gain
Copy Number
Allele State
Allele Origin
Probe Count
Merged StatusS
Merged Variants
Supporting Variantsnssv1535169
SamplesMS12050
Known GenesPLA2G4A, PTGS2
Method
Analysis
PlatformIllumina HumanHap 610 Quad + Illumina HumanHap 1MduoV3
Comments
ReferenceXu_et_al_2011
Pubmed ID21882294
Accession Number(s)nsv872590
Frequency
Sample Size6533
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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