A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv512984



Internal ID15852406
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:2781387..2782102hg38UCSC Ensembl
Outerchr9:2781387..2782102hg19UCSC Ensembl
Outerchr9:2771387..2772102hg18UCSC Ensembl
Cytoband9p24.2
Allele length
AssemblyAllele length
hg381078
hg191078
hg181078
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv625639
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)nsv512984
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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