A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv556377



Internal ID15997100
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:107602007..107695859hg38UCSC Ensembl
Innerchr11:107472733..107566585hg19UCSC Ensembl
Innerchr11:106977943..107071795hg18UCSC Ensembl
Cytoband11q22.3
Allele length
AssemblyAllele length
hg3893853
hg1993853
hg1893853
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv784207
Samples
Known GenesELMOD1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv556377
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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