A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv555090



Internal ID16342499
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:55937346..55962275hg38UCSC Ensembl
Innerchr11:55704822..55729751hg19UCSC Ensembl
Innerchr11:55461398..55486327hg18UCSC Ensembl
Cytoband11q11
Allele length
AssemblyAllele length
hg3824930
hg1924930
hg1824930
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1947n54
Supporting Variantsnssv1174796, nssv776854, nssv776853
Samples1780854261_A
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv555090
Frequency
Sample Size17421
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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