A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv896545



Internal ID6303556
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:541930..705404hg19UCSC Ensembl
Outerchr11:521302..710558hg19UCSC Ensembl
Innerchr11:531930..695404hg18UCSC Ensembl
Outerchr11:511302..700558hg18UCSC Ensembl
Cytoband11p15.5
Allele length
AssemblyAllele length
hg19n/a
hg18n/a
Variant TypeCNV Loss
Copy Number
Allele State
Allele Origin
Probe Count
Merged StatusS
Merged Variants
Supporting Variantsnssv1571905
SamplesIS32841
Known GenesC11orf35, CDHR5, DEAF1, DRD4, EPS8L2, HRAS, IRF7, LOC143666, LRRC56, MIR210, MIR210HG, PHRF1, RASSF7, SCT, TMEM80
Method
Analysis
PlatformIllumina HumanHap 610 Quad + Illumina HumanHap 1MduoV3
Comments
ReferenceXu_et_al_2011
Pubmed ID21882294
Accession Number(s)nsv896545
Frequency
Sample Size6533
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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