A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv897018



Internal ID6304029
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:17405333..17415881hg19UCSC Ensembl
Outerchr11:17403639..17417337hg19UCSC Ensembl
Innerchr11:17361909..17372457hg18UCSC Ensembl
Outerchr11:17360215..17373913hg18UCSC Ensembl
Cytoband11p15.1
Allele length
AssemblyAllele length
hg19n/a
hg18n/a
Variant TypeCNV Loss
Copy Number
Allele State
Allele Origin
Probe Count
Merged StatusS
Merged Variants
Supporting Variantsnssv1510002
SamplesSP54956
Known GenesABCC8, KCNJ11
Method
Analysis
PlatformIllumina HumanHap 610 Quad + Illumina HumanHap 1MduoV3
Comments
ReferenceXu_et_al_2011
Pubmed ID21882294
Accession Number(s)nsv897018
Frequency
Sample Size6533
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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