A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv778613



Internal ID15725883
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:68025546..68049469hg38UCSC Ensembl
Innerchr11:67793014..67816936hg19UCSC Ensembl
Innerchr11:67549590..67573512hg18UCSC Ensembl
Cytoband11q13.2
Allele length
AssemblyAllele length
hg3823924
hg1923923
hg1823923
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv555280
Supporting Variants
Samples
Known GenesALDH3B1, 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)nssv778613
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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