A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv511409



Internal ID15850834
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:135587331..135588299hg38UCSC Ensembl
Outerchr9:135584977..135588640hg38UCSC Ensembl
Innerchr9:138479177..138480145hg19UCSC Ensembl
Outerchr9:138476823..138480486hg19UCSC Ensembl
Innerchr9:137618998..137619966hg18UCSC Ensembl
Outerchr9:137616644..137620307hg18UCSC Ensembl
Cytoband9q34.3
Allele length
AssemblyAllele length
hg383664
hg193664
hg183664
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv626017
Samples1
Known GenesLOC100130954
MethodSNP array
AnalysisAnalysis of HGMDFN090 by Illumina HumanOmni1 Quad SNP array
PlatformGPL8882
Comments
ReferenceArlt_et_al_2011
Pubmed ID21212237
Accession Number(s)nsv511409
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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