A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv511851



Internal ID15851276
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr6:14743165..14745552hg38UCSC Ensembl
Outerchr6:14743396..14745783hg19UCSC Ensembl
Outerchr6:14851375..14853762hg18UCSC Ensembl
Cytoband6p23
Allele length
AssemblyAllele length
hg382388
hg192388
hg182388
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv624381
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)nsv511851
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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