A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv554076



Internal ID16341485
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:39051419..39117561hg38UCSC Ensembl
Innerchr11:39072969..39139111hg19UCSC Ensembl
Innerchr11:39029545..39095687hg18UCSC Ensembl
Cytoband11p12
Allele length
AssemblyAllele length
hg3866143
hg1966143
hg1866143
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1757n54
Supporting Variantsnssv771158
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv554076
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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