A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1039646



Internal ID18782177
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:135010963..135083283hg38UCSC Ensembl
Innerchr9:137902809..137975129hg19UCSC Ensembl
Innerchr9:137042630..137114950hg18UCSC Ensembl
Cytoband9q34.3
Allele length
AssemblyAllele length
hg3872321
hg1972321
hg1872321
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3759841
Samples
Known GenesOLFM1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1039646
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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