A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv626030



Internal ID15849563
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 StatusS
Merged Variantsnsv511421
Supporting Variants
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)nssv626030
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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