A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv902389



Internal ID6264316
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:105100021..105348552hg19UCSC Ensembl
Outerchr14:105092479..105366499hg19UCSC Ensembl
Innerchr14:104171066..104419597hg18UCSC Ensembl
Outerchr14:104163524..104437544hg18UCSC Ensembl
Cytoband14q32.33
Allele length
AssemblyAllele length
hg19n/a
hg18n/a
Variant TypeCNV Loss
Copy Number
Allele State
Allele Origin
Probe Count
Merged StatusS
Merged Variants
Supporting Variantsnssv1549866
SamplesMS18276
Known GenesADSSL1, AKT1, INF2, KIAA0284, MGC23270, MIR4710, SIVA1, ZBTB42
Method
Analysis
PlatformIllumina HumanHap 610 Quad + Illumina HumanHap 1MduoV3
Comments
ReferenceXu_et_al_2011
Pubmed ID21882294
Accession Number(s)nsv902389
Frequency
Sample Size6533
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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