A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv912154



Internal ID6274081
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:45923653..46056620hg19UCSC Ensembl
Outerchr19:45920796..46059364hg19UCSC Ensembl
Innerchr19:50615493..50748460hg18UCSC Ensembl
Outerchr19:50612636..50751204hg18UCSC Ensembl
Cytoband19q13.32
Allele length
AssemblyAllele length
hg19n/a
hg18n/a
Variant TypeCNV Loss
Copy Number
Allele State
Allele Origin
Probe Count
Merged StatusS
Merged Variants
Supporting Variantsnssv1592455
SamplesIS39233
Known GenesERCC1, FOSB, OPA3, PPM1N, RTN2, VASP
Method
Analysis
PlatformIllumina HumanHap 610 Quad + Illumina HumanHap 1MduoV3
Comments
ReferenceXu_et_al_2011
Pubmed ID21882294
Accession Number(s)nsv912154
Frequency
Sample Size6533
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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