A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv890632



Internal ID6297643
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:19818436..19844222hg19UCSC Ensembl
Outerchr8:19816371..19853146hg19UCSC Ensembl
Innerchr8:19862716..19888502hg18UCSC Ensembl
Outerchr8:19860651..19897426hg18UCSC Ensembl
Cytoband8p21.3
Allele length
AssemblyAllele length
hg19n/a
hg18n/a
Variant TypeCNV Loss
Copy Number
Allele State
Allele Origin
Probe Count
Merged StatusS
Merged Variants
Supporting Variantsnssv1522736
SamplesSP53407
Known GenesLPL
Method
Analysis
PlatformIllumina HumanHap 610 Quad + Illumina HumanHap 1MduoV3
Comments
ReferenceXu_et_al_2011
Pubmed ID21882294
Accession Number(s)nsv890632
Frequency
Sample Size6533
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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