A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3759840



Internal ID19058121
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 StatusS
Merged Variantsnsv1043726
Supporting Variants
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)nssv3759840
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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