A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv896929



Internal ID6303940
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:5196450..5268797hg19UCSC Ensembl
Outerchr11:5192095..5271671hg19UCSC Ensembl
Innerchr11:5153026..5225373hg18UCSC Ensembl
Outerchr11:5148671..5228247hg18UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg19n/a
hg18n/a
Variant TypeCNV Loss
Copy Number
Allele State
Allele Origin
Probe Count
Merged StatusS
Merged Variants
Supporting Variantsnssv1523320
SamplesSP53947
Known GenesHBB, HBBP1, HBD, HBG1, OR51V1
Method
Analysis
PlatformIllumina HumanHap 610 Quad + Illumina HumanHap 1MduoV3
Comments
ReferenceXu_et_al_2011
Pubmed ID21882294
Accession Number(s)nsv896929
Frequency
Sample Size6533
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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