A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv894816



Internal ID6301827
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:6176112..6183805hg19UCSC Ensembl
Outerchr10:6173416..6190343hg19UCSC Ensembl
Innerchr10:6216118..6223811hg18UCSC Ensembl
Outerchr10:6213422..6230349hg18UCSC Ensembl
Cytoband10p15.1
Allele length
AssemblyAllele length
hg19n/a
hg18n/a
Variant TypeCNV Loss
Copy Number
Allele State
Allele Origin
Probe Count
Merged StatusS
Merged Variants
Supporting Variantsnssv1532441
SamplesMS10769
Known GenesPFKFB3
Method
Analysis
PlatformIllumina HumanHap 610 Quad + Illumina HumanHap 1MduoV3
Comments
ReferenceXu_et_al_2011
Pubmed ID21882294
Accession Number(s)nsv894816
Frequency
Sample Size6533
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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