A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1043726



Internal ID18786257
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:134566621..135388584hg38UCSC Ensembl
Innerchr9:137458467..138280430hg19UCSC Ensembl
Innerchr9:136598288..137420251hg18UCSC Ensembl
Cytoband9q34.2
Allele length
AssemblyAllele length
hg38821964
hg19821964
hg18821964
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3759840
Samples
Known GenesC9orf62, COL5A1, FCN1, FCN2, LOC101448202, LOC401557, MIR3689A, MIR3689B, MIR3689C, MIR3689D1, MIR3689D2, MIR3689E, MIR3689F, OLFM1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1043726
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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