A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv553297



Internal ID16340706
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:5739829..5740399hg38UCSC Ensembl
Innerchr11:5761059..5761629hg19UCSC Ensembl
Innerchr11:5717635..5718205hg18UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg38571
hg19571
hg18571
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1613n54
Supporting Variantsnssv765890
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv553297
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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