A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv513433



Internal ID15852855
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:74552230..74552499hg38UCSC Ensembl
Outerchr15:74844571..74844840hg19UCSC Ensembl
Outerchr15:72631624..72631893hg18UCSC Ensembl
Cytoband15q24.1
Allele length
AssemblyAllele length
hg381997
hg191997
hg181997
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv625834
Samples1
Known GenesARID3B
MethodSequencing
AnalysisAnalysis of HGMDFN090 by Illumina Genome Analyzer mate pairs
PlatformNot reported
Comments
ReferenceArlt_et_al_2011
Pubmed ID21212237
Accession Number(s)nsv513433
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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