A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv511911



Internal ID15504650
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr6:111902555..111908962hg38UCSC Ensembl
Outerchr6:112223758..112230165hg19UCSC Ensembl
Outerchr6:112330451..112336858hg18UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg386408
hg196408
hg186408
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv624447
Samples1
Known Genes
MethodSequencing
AnalysisAnalysis of HGMDFN090 by Illumina Genome Analyzer mate pairs
PlatformNot reported
Comments
ReferenceArlt_et_al_2011
Pubmed ID21212237
Accession Number(s)nsv511911
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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