A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv902190



Internal ID6264117
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:92499348..92600798hg19UCSC Ensembl
Outerchr14:92493436..92627138hg19UCSC Ensembl
Innerchr14:91569101..91670551hg18UCSC Ensembl
Outerchr14:91563189..91696891hg18UCSC Ensembl
Cytoband14q32.12
Allele length
AssemblyAllele length
hg19n/a
hg18n/a
Variant TypeCNV Loss
Copy Number
Allele State
Allele Origin
Probe Count
Merged StatusS
Merged Variants
Supporting Variantsnssv1579881
SamplesIS35181
Known GenesATXN3, CPSF2, NDUFB1, TRIP11
Method
Analysis
PlatformIllumina HumanHap 610 Quad + Illumina HumanHap 1MduoV3
Comments
ReferenceXu_et_al_2011
Pubmed ID21882294
Accession Number(s)nsv902190
Frequency
Sample Size6533
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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