A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv879011



Internal ID6286022
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:52810307..53165610hg19UCSC Ensembl
Outerchr4:52801096..53198197hg19UCSC Ensembl
Innerchr4:52505064..52860367hg18UCSC Ensembl
Outerchr4:52495853..52892954hg18UCSC Ensembl
Cytoband4q12
Allele length
AssemblyAllele length
hg19n/a
hg18n/a
Variant TypeCNV Gain
Copy Number
Allele State
Allele Origin
Probe Count
Merged StatusS
Merged Variants
Supporting Variantsnssv1548982
SamplesMS17970
Known GenesLRRC66, SGCB, SPATA18
Method
Analysis
PlatformIllumina HumanHap 610 Quad + Illumina HumanHap 1MduoV3
Comments
ReferenceXu_et_al_2011
Pubmed ID21882294
Accession Number(s)nsv879011
Frequency
Sample Size6533
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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