A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv555377



Internal ID16342786
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:70158589..70186722hg38UCSC Ensembl
Innerchr11:70004695..70032828hg19UCSC Ensembl
Innerchr11:69682343..69710476hg18UCSC Ensembl
Cytoband11q13.3
Allele length
AssemblyAllele length
hg3828134
hg1928134
hg1828134
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv778916
Samples
Known GenesANO1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv555377
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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