A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv555211



Internal ID16342620
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:65500998..65504854hg38UCSC Ensembl
Innerchr11:65268469..65272325hg19UCSC Ensembl
Innerchr11:65025045..65028901hg18UCSC Ensembl
Cytoband11q13.1
Allele length
AssemblyAllele length
hg383857
hg193857
hg183857
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv777175
Samples
Known GenesMALAT1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv555211
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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