A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv511878



Internal ID15851303
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr6:34069201..34072503hg38UCSC Ensembl
Outerchr6:34036978..34040280hg19UCSC Ensembl
Outerchr6:34144956..34148258hg18UCSC Ensembl
Cytoband6p21.31
Allele length
AssemblyAllele length
hg383303
hg193303
hg183303
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv624410
Samples1
Known GenesGRM4
MethodSequencing
AnalysisAnalysis of HGMDFN090 by Illumina Genome Analyzer mate pairs
PlatformNot reported
Comments
ReferenceArlt_et_al_2011
Pubmed ID21212237
Accession Number(s)nsv511878
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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