A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv511408



Internal ID15850833
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:137102262..137103192hg38UCSC Ensembl
Outerchr9:137100613..137106120hg38UCSC Ensembl
Innerchr9:139996714..139997644hg19UCSC Ensembl
Outerchr9:139995065..140000572hg19UCSC Ensembl
Innerchr9:139116535..139117465hg18UCSC Ensembl
Outerchr9:139114886..139120393hg18UCSC Ensembl
Cytoband9q34.3
Allele length
AssemblyAllele length
hg385508
hg195508
hg185508
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv626016
Samples1
Known GenesMAN1B1
MethodSNP array
AnalysisAnalysis of HGMDFN090 by Illumina HumanOmni1 Quad SNP array
PlatformGPL8882
Comments
ReferenceArlt_et_al_2011
Pubmed ID21212237
Accession Number(s)nsv511408
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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