A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv582533



Internal ID16369942
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:100469689..100486922hg38UCSC Ensembl
Innerchr2:101086151..101103384hg19UCSC Ensembl
Innerchr2:100452583..100469816hg18UCSC Ensembl
Cytoband2q11.2
Allele length
AssemblyAllele length
hg3817234
hg1917234
hg1817234
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv914555
Samples
Known GenesNMS
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv582533
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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