A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv512142



Internal ID15851567
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:6209877..6210995hg38UCSC Ensembl
Outerchr10:6251840..6252958hg19UCSC Ensembl
Outerchr10:6291846..6292964hg18UCSC Ensembl
Cytoband10p15.1
Allele length
AssemblyAllele length
hg381119
hg191119
hg181119
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv624703
Samples1
Known GenesPFKFB3
MethodSequencing
AnalysisAnalysis of HGMDFN090 by Illumina Genome Analyzer mate pairs
PlatformNot reported
Comments
ReferenceArlt_et_al_2011
Pubmed ID21212237
Accession Number(s)nsv512142
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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