A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv895378



Internal ID6302389
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:50804578..50953830hg19UCSC Ensembl
Outerchr10:50801342..50955649hg19UCSC Ensembl
Innerchr10:50474584..50623836hg18UCSC Ensembl
Outerchr10:50471348..50625655hg18UCSC Ensembl
Cytoband10q11.23
Allele length
AssemblyAllele length
hg19n/a
hg18n/a
Variant TypeCNV Gain
Copy Number
Allele State
Allele Origin
Probe Count
Merged StatusS
Merged Variants
Supporting Variantsnssv1518273
SamplesSP57481
Known GenesC10orf53, CHAT, OGDHL, SLC18A3
Method
Analysis
PlatformIllumina HumanHap 610 Quad + Illumina HumanHap 1MduoV3
Comments
ReferenceXu_et_al_2011
Pubmed ID21882294
Accession Number(s)nsv895378
Frequency
Sample Size6533
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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