A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv887298



Internal ID6294309
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:2568770..2629020hg19UCSC Ensembl
Outerchr7:2556157..2640141hg19UCSC Ensembl
Innerchr7:2535296..2595546hg18UCSC Ensembl
Outerchr7:2522683..2606667hg18UCSC Ensembl
Cytoband7p22.2
Allele length
AssemblyAllele length
hg19n/a
hg18n/a
Variant TypeCNV Loss
Copy Number
Allele State
Allele Origin
Probe Count
Merged StatusS
Merged Variants
Supporting Variantsnssv1593139
SamplesIS39363
Known GenesBRAT1, IQCE, LFNG, MIR4648
Method
Analysis
PlatformIllumina HumanHap 610 Quad + Illumina HumanHap 1MduoV3
Comments
ReferenceXu_et_al_2011
Pubmed ID21882294
Accession Number(s)nsv887298
Frequency
Sample Size6533
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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