A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv877389



Internal ID6284400
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:121901382..121903936hg19UCSC Ensembl
Outerchr3:121900649..121904054hg19UCSC Ensembl
Innerchr3:123384072..123386626hg18UCSC Ensembl
Outerchr3:123383339..123386744hg18UCSC Ensembl
Cytoband3q13.33
Allele length
AssemblyAllele length
hg19n/a
hg18n/a
Variant TypeCNV Loss
Copy Number
Allele State
Allele Origin
Probe Count
Merged StatusS
Merged Variants
Supporting Variantsnssv1507565
SamplesSP54684
Known GenesCASR
Method
Analysis
PlatformIllumina HumanHap 610 Quad + Illumina HumanHap 1MduoV3
Comments
ReferenceXu_et_al_2011
Pubmed ID21882294
Accession Number(s)nsv877389
Frequency
Sample Size6533
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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