A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv584226



Internal ID16371635
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:203317361..203326184hg38UCSC Ensembl
Innerchr2:204182084..204190907hg19UCSC Ensembl
Innerchr2:203890329..203899152hg18UCSC Ensembl
Cytoband2q33.2
Allele length
AssemblyAllele length
hg388824
hg198824
hg188824
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7261n54
Supporting Variantsnssv930570
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv584226
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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