A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv584614



Internal ID16372023
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:228394886..228401669hg38UCSC Ensembl
Innerchr2:229259602..229266385hg19UCSC Ensembl
Innerchr2:228967846..228974629hg18UCSC Ensembl
Cytoband2q36.3
Allele length
AssemblyAllele length
hg386784
hg196784
hg186784
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv933326
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv584614
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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