A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv511421



Internal ID15850846
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:88534316..88535071hg38UCSC Ensembl
Outerchr9:88534264..88535546hg38UCSC Ensembl
Innerchr9:91149231..91149986hg19UCSC Ensembl
Outerchr9:91149179..91150461hg19UCSC Ensembl
Innerchr9:90339051..90339806hg18UCSC Ensembl
Outerchr9:90338999..90340281hg18UCSC Ensembl
Cytoband9q22.1
Allele length
AssemblyAllele length
hg381283
hg191283
hg181283
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv626030
Samples1
Known GenesNXNL2
MethodSNP array
AnalysisAnalysis of HGMDFN090 by Illumina HumanOmni1 Quad SNP array
PlatformGPL8882
Comments
ReferenceArlt_et_al_2011
Pubmed ID21212237
Accession Number(s)nsv511421
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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