A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv555281



Internal ID15996004
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:68029224..68053569hg38UCSC Ensembl
Innerchr11:67796691..67821036hg19UCSC Ensembl
Innerchr11:67553267..67577612hg18UCSC Ensembl
Cytoband11q13.2
Allele length
AssemblyAllele length
hg3824346
hg1924346
hg1824346
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1983n54
Supporting Variantsnssv778614
Samples
Known GenesALDH3B1, CHKA, MIR4691, MIR6753, MIR7113, NDUFS8, TCIRG1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv555281
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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