A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv512126



Internal ID15851551
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:134848061..134850022hg38UCSC Ensembl
Outerchr9:137739907..137741868hg19UCSC Ensembl
Outerchr9:136879728..136881689hg18UCSC Ensembl
Cytoband9q34.3
Allele length
AssemblyAllele length
hg381962
hg191962
hg181962
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv624685
Samples1
Known GenesLOC101448202, MIR3689A, MIR3689C, MIR3689D1
MethodSequencing
AnalysisAnalysis of HGMDFN090 by Illumina Genome Analyzer mate pairs
PlatformNot reported
Comments
ReferenceArlt_et_al_2011
Pubmed ID21212237
Accession Number(s)nsv512126
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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