A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv553408



Internal ID16340817
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:7724805..7816894hg38UCSC Ensembl
Innerchr11:7746352..7838441hg19UCSC Ensembl
Innerchr11:7702928..7795017hg18UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg3892090
hg1992090
hg1892090
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv766940
Samples
Known GenesOR5P2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv553408
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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