A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv901616



Internal ID6263543
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:35868514..35877721hg19UCSC Ensembl
Outerchr14:35862404..35883678hg19UCSC Ensembl
Innerchr14:34938265..34947472hg18UCSC Ensembl
Outerchr14:34932155..34953429hg18UCSC Ensembl
Cytoband14q13.2
Allele length
AssemblyAllele length
hg19n/a
hg18n/a
Variant TypeCNV Loss
Copy Number
Allele State
Allele Origin
Probe Count
Merged StatusS
Merged Variants
Supporting Variantsnssv1510070
SamplesSP54956
Known GenesNFKBIA
Method
Analysis
PlatformIllumina HumanHap 610 Quad + Illumina HumanHap 1MduoV3
Comments
ReferenceXu_et_al_2011
Pubmed ID21882294
Accession Number(s)nsv901616
Frequency
Sample Size6533
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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