A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv553367



Internal ID16340776
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:6095744..6099847hg38UCSC Ensembl
Innerchr11:6116974..6121077hg19UCSC Ensembl
Innerchr11:6073550..6077653hg18UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg384104
hg194104
hg184104
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1624n54
Supporting Variantsnssv766324, nssv766323
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv553367
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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