A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv909288



Internal ID6271215
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:285953..2425172hg19UCSC Ensembl
Outerchr18:277763..2436748hg19UCSC Ensembl
Innerchr18:275953..2415172hg18UCSC Ensembl
Outerchr18:267763..2426748hg18UCSC Ensembl
Cytoband18p11.32
Allele length
AssemblyAllele length
hg19n/a
hg18n/a
Variant TypeCNV Loss
Copy Number
Allele State
Allele Origin
Probe Count
Merged StatusS
Merged Variants
Supporting Variantsnssv1559589
SamplesMS24046
Known GenesADCYAP1, C18orf56, CETN1, CLUL1, COLEC12, ENOSF1, LINC00470, TYMS, YES1
Method
Analysis
PlatformIllumina HumanHap 610 Quad + Illumina HumanHap 1MduoV3
Comments
ReferenceXu_et_al_2011
Pubmed ID21882294
Accession Number(s)nsv909288
Frequency
Sample Size6533
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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