A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv513018



Internal ID15852440
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:114083584..114084043hg38UCSC Ensembl
Outerchr10:115843343..115843802hg19UCSC Ensembl
Outerchr10:115833333..115833792hg18UCSC Ensembl
Cytoband10q25.3
Allele length
AssemblyAllele length
hg381727
hg191727
hg181727
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv625676
Samples1
Known Genes
MethodSequencing
AnalysisAnalysis of HGMDFN090 by Illumina Genome Analyzer mate pairs
PlatformNot reported
Comments
ReferenceArlt_et_al_2011
Pubmed ID21212237
Accession Number(s)nsv513018
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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