A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1045766



Internal ID18788297
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:122107328..122133221hg38UCSC Ensembl
Innerchr9:124869607..124895500hg19UCSC Ensembl
Innerchr9:123909428..123935321hg18UCSC Ensembl
Cytoband9q33.2
Allele length
AssemblyAllele length
hg3825894
hg1925894
hg1825894
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7714n100
Supporting Variantsnssv3695223
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)nsv1045766
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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