A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv553084



Internal ID15993807
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:2299609..2300906hg38UCSC Ensembl
Innerchr11:2320839..2322136hg19UCSC Ensembl
Innerchr11:2277415..2278712hg18UCSC Ensembl
Cytoband11p15.5
Allele length
AssemblyAllele length
hg381298
hg191298
hg181298
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv764501, nssv764500, nssv764505, nssv764502, nssv764504, nssv764503
Samples
Known GenesC11orf21
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv553084
Frequency
Sample Size17421
Observed Gain5
Observed Loss1
Observed Complex0
Frequencyn/a


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