A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv881299



Internal ID6288310
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:175410435..175414678hg19UCSC Ensembl
Outerchr4:175403673..175415442hg19UCSC Ensembl
Innerchr4:175647010..175651253hg18UCSC Ensembl
Outerchr4:175640248..175652017hg18UCSC Ensembl
Cytoband4q34.1
Allele length
AssemblyAllele length
hg19n/a
hg18n/a
Variant TypeCNV Loss
Copy Number
Allele State
Allele Origin
Probe Count
Merged StatusS
Merged Variants
Supporting Variantsnssv1515239
SamplesSP56143
Known GenesHPGD
Method
Analysis
PlatformIllumina HumanHap 610 Quad + Illumina HumanHap 1MduoV3
Comments
ReferenceXu_et_al_2011
Pubmed ID21882294
Accession Number(s)nsv881299
Frequency
Sample Size6533
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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