A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv880238



Internal ID6287249
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:147473314..147595984hg19UCSC Ensembl
Outerchr4:147469559..147617963hg19UCSC Ensembl
Innerchr4:147692764..147815434hg18UCSC Ensembl
Outerchr4:147689009..147837413hg18UCSC Ensembl
Cytoband4q31.22
Allele length
AssemblyAllele length
hg19n/a
hg18n/a
Variant TypeCNV Loss
Copy Number
Allele State
Allele Origin
Probe Count
Merged StatusS
Merged Variants
Supporting Variantsnssv1597416
SamplesIS41292
Known GenesPOU4F2
Method
Analysis
PlatformIllumina HumanHap 610 Quad + Illumina HumanHap 1MduoV3
Comments
ReferenceXu_et_al_2011
Pubmed ID21882294
Accession Number(s)nsv880238
Frequency
Sample Size6533
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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