A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv584561



Internal ID16371970
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:226284863..226302119hg38UCSC Ensembl
Innerchr2:227149579..227166835hg19UCSC Ensembl
Innerchr2:226857823..226875079hg18UCSC Ensembl
Cytoband2q36.3
Allele length
AssemblyAllele length
hg3817257
hg1917257
hg1817257
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7310n54
Supporting Variantsnssv932912
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv584561
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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