A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv553121



Internal ID16340530
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:2917730..2928631hg38UCSC Ensembl
Innerchr11:2938960..2949861hg19UCSC Ensembl
Innerchr11:2895536..2906437hg18UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg3810902
hg1910902
hg1810902
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv764548
Samples
Known GenesPHLDA2, SLC22A18
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv553121
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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