A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv511431



Internal ID15850856
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:134848959..134850820hg38UCSC Ensembl
Outerchr9:134848134..134851084hg38UCSC Ensembl
Innerchr9:137740805..137742666hg19UCSC Ensembl
Outerchr9:137739980..137742930hg19UCSC Ensembl
Innerchr9:136880626..136882487hg18UCSC Ensembl
Outerchr9:136879801..136882751hg18UCSC Ensembl
Cytoband9q34.3
Allele length
AssemblyAllele length
hg382951
hg192951
hg182951
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv626042
Samples1
Known GenesLOC101448202, MIR3689A, MIR3689B, MIR3689C, MIR3689D1, MIR3689D2, MIR3689E, MIR3689F
MethodSNP array
AnalysisAnalysis of HGMDFN090 by Illumina HumanOmni1 Quad SNP array
PlatformGPL8882
Comments
ReferenceArlt_et_al_2011
Pubmed ID21212237
Accession Number(s)nsv511431
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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