A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv511879



Internal ID15851304
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr6:35135891..35138311hg38UCSC Ensembl
Outerchr6:35103668..35106088hg19UCSC Ensembl
Outerchr6:35211646..35214066hg18UCSC Ensembl
Cytoband6p21.31
Allele length
AssemblyAllele length
hg382421
hg192421
hg182421
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv624412
Samples1
Known GenesTCP11
MethodSequencing
AnalysisAnalysis of HGMDFN090 by Illumina Genome Analyzer mate pairs
PlatformNot reported
Comments
ReferenceArlt_et_al_2011
Pubmed ID21212237
Accession Number(s)nsv511879
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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