A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv584816



Internal ID16372225
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:240644259..240653740hg38UCSC Ensembl
Innerchr2:241583676..241593157hg19UCSC Ensembl
Innerchr2:241232349..241241830hg18UCSC Ensembl
Cytoband2q37.3
Allele length
AssemblyAllele length
hg389482
hg199482
hg189482
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1151192
SamplesHGDP00684
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv584816
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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