A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv553291



Internal ID16340700
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:5738942..5741619hg38UCSC Ensembl
Innerchr11:5760172..5762849hg19UCSC Ensembl
Innerchr11:5716748..5719425hg18UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg382678
hg192678
hg182678
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1611n54
Supporting Variantsnssv765884
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv553291
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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