A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv511924



Internal ID15851349
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr6:164341146..164656366hg38UCSC Ensembl
Outerchr6:164762179..165077399hg19UCSC Ensembl
Outerchr6:164682169..164997389hg18UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg38315221
hg19315221
hg18315221
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv624461
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)nsv511924
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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