A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv513741



Internal ID15853162
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:32718089..32733479hg38UCSC Ensembl
Outerchr9:32718087..32733477hg19UCSC Ensembl
Outerchr9:32708087..32723477hg18UCSC Ensembl
Cytoband9p21.1
Allele length
AssemblyAllele length
hg3815391
hg1915391
hg1815391
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv626993
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)nsv513741
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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