A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv556228



Internal ID15996951
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:106664983..106705931hg38UCSC Ensembl
Innerchr11:106535709..106576657hg19UCSC Ensembl
Innerchr11:106040919..106081867hg18UCSC Ensembl
Cytoband11q22.3
Allele length
AssemblyAllele length
hg3840949
hg1940949
hg1840949
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv783383
Samples
Known GenesGUCY1A2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv556228
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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