A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv881601



Internal ID6288612
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:155511425..155533169hg19UCSC Ensembl
Outerchr4:155510717..155533540hg19UCSC Ensembl
Innerchr4:155730875..155752619hg18UCSC Ensembl
Outerchr4:155730167..155752990hg18UCSC Ensembl
Cytoband4q31.3
Allele length
AssemblyAllele length
hg19n/a
hg18n/a
Variant TypeCNV Loss
Copy Number
Allele State
Allele Origin
Probe Count
Merged StatusS
Merged Variants
Supporting Variantsnssv1504684
SamplesSP52708
Known GenesFGA, FGG
Method
Analysis
PlatformIllumina HumanHap 610 Quad + Illumina HumanHap 1MduoV3
Comments
ReferenceXu_et_al_2011
Pubmed ID21882294
Accession Number(s)nsv881601
Frequency
Sample Size6533
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer