A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv513296



Internal ID15852718
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr6:5896384..5899860hg38UCSC Ensembl
Outerchr6:5896617..5900093hg19UCSC Ensembl
Outerchr6:5841616..5845092hg18UCSC Ensembl
Cytoband6p25.1
Allele length
AssemblyAllele length
hg383477
hg193477
hg183477
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv626806
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)nsv513296
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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