A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv584550



Internal ID16371959
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:223680101..223751439hg38UCSC Ensembl
Innerchr2:224544818..224616156hg19UCSC Ensembl
Innerchr2:224253062..224324400hg18UCSC Ensembl
Cytoband2q36.1
Allele length
AssemblyAllele length
hg3871339
hg1971339
hg1871339
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1151350
Samples1780854517_A
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv584550
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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