A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv513016



Internal ID15852438
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:101854868..101855348hg38UCSC Ensembl
Outerchr10:103614625..103615105hg19UCSC Ensembl
Outerchr10:103604615..103605095hg18UCSC Ensembl
Cytoband10q24.32
Allele length
AssemblyAllele length
hg381418
hg191418
hg181418
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv625674
Samples1
Known GenesC10orf76
MethodSequencing
AnalysisAnalysis of HGMDFN090 by Illumina Genome Analyzer mate pairs
PlatformNot reported
Comments
ReferenceArlt_et_al_2011
Pubmed ID21212237
Accession Number(s)nsv513016
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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