A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1038490



Internal ID18781021
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:122107328..122135503hg38UCSC Ensembl
Innerchr9:124869607..124897782hg19UCSC Ensembl
Innerchr9:123909428..123937603hg18UCSC Ensembl
Cytoband9q33.2
Allele length
AssemblyAllele length
hg3828176
hg1928176
hg1828176
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7714n100
Supporting Variantsnssv3695224
Samples
Known GenesMIR4478
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1038490
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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