A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv831876



Internal ID6157600
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:54492511..54649392hg19UCSC Ensembl
Outerchr10:54162517..54319398hg18UCSC Ensembl
Outerchr10:54162517..54319398hg17UCSC Ensembl
Cytoband10q21.1
Allele length
AssemblyAllele length
hg19n/a
hg18n/a
hg17n/a
Variant TypeCNV Gain
Copy Number
Allele State
Allele Origin
Probe Count
Merged StatusS
Merged Variants
Supporting Variantsnssv1448507
Samples
Known GenesMBL2
Method
Analysis
PlatformSMRT Whole Genome Tile Path BAC CGH Array
Comments
ReferenceWong_et_al_2007
Pubmed ID17160897
Accession Number(s)nsv831876
Frequency
Sample Size95
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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