A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2785193



Internal ID15808742
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:18928573..18939269hg38UCSC Ensembl
Innerchr11:18950120..18960816hg19UCSC Ensembl
Innerchr11:18906696..18917392hg18UCSC Ensembl
Cytoband11p15.1
Allele length
AssemblyAllele length
hg3810697
hg1910697
hg1810697
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv514600
Supporting Variants
SamplesNA21634
Known GenesMRGPRX1
MethodOligo aCGH
AnalysisADM2 threshold = 5
PlatformAgilent Eichler Human CNP 180K v3.0
Comments
ReferenceCampbell_et_al_2011
Pubmed ID21397061
Accession Number(s)nssv2785193
Frequency
Sample Size2366
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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