A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv553940



Internal ID16341349
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:29157407..29199747hg38UCSC Ensembl
Innerchr11:29178954..29221294hg19UCSC Ensembl
Innerchr11:29135530..29177870hg18UCSC Ensembl
Cytoband11p14.1
Allele length
AssemblyAllele length
hg3842341
hg1942341
hg1842341
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1733n54
Supporting Variantsnssv770387
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv553940
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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