A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv902208



Internal ID6264135
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:95202487..95250756hg19UCSC Ensembl
Outerchr14:95193558..95253783hg19UCSC Ensembl
Innerchr14:94272240..94320509hg18UCSC Ensembl
Outerchr14:94263311..94323536hg18UCSC Ensembl
Cytoband14q32.13
Allele length
AssemblyAllele length
hg19n/a
hg18n/a
Variant TypeCNV Gain
Copy Number
Allele State
Allele Origin
Probe Count
Merged StatusS
Merged Variants
Supporting Variantsnssv1523389
SamplesSP53999
Known GenesGSC
Method
Analysis
PlatformIllumina HumanHap 610 Quad + Illumina HumanHap 1MduoV3
Comments
ReferenceXu_et_al_2011
Pubmed ID21882294
Accession Number(s)nsv902208
Frequency
Sample Size6533
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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