A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv511928



Internal ID15851353
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr6:168356691..168359772hg38UCSC Ensembl
Outerchr6:168757371..168760452hg19UCSC Ensembl
Outerchr6:168500220..168503301hg18UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg383082
hg193082
hg183082
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv624465
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)nsv511928
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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