A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv512193



Internal ID15504932
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:131110728..131114606hg38UCSC Ensembl
Outerchr10:132908991..132912869hg19UCSC Ensembl
Outerchr10:132798981..132802859hg18UCSC Ensembl
Cytoband10q26.3
Allele length
AssemblyAllele length
hg383879
hg193879
hg183879
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv624760
Samples1
Known GenesTCERG1L
MethodSequencing
AnalysisAnalysis of HGMDFN090 by Illumina Genome Analyzer mate pairs
PlatformNot reported
Comments
ReferenceArlt_et_al_2011
Pubmed ID21212237
Accession Number(s)nsv512193
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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