A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv904343



Internal ID6266270
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:73402903..73766072hg19UCSC Ensembl
Outerchr15:73396760..73775043hg19UCSC Ensembl
Innerchr15:71189956..71553125hg18UCSC Ensembl
Outerchr15:71183813..71562096hg18UCSC Ensembl
Cytoband15q24.1
Allele length
AssemblyAllele length
hg19n/a
hg18n/a
Variant TypeCNV Gain
Copy Number
Allele State
Allele Origin
Probe Count
Merged StatusS
Merged Variants
Supporting Variantsnssv1508747
SamplesSP54665
Known GenesC15orf60, HCN4, NEO1
Method
Analysis
PlatformIllumina HumanHap 610 Quad + Illumina HumanHap 1MduoV3
Comments
ReferenceXu_et_al_2011
Pubmed ID21882294
Accession Number(s)nsv904343
Frequency
Sample Size6533
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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