A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1046307



Internal ID18788838
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:130029993..130219186hg38UCSC Ensembl
Innerchr9:132792272..132981465hg19UCSC Ensembl
Innerchr9:131832093..132021286hg18UCSC Ensembl
Cytoband9q34.11
Allele length
AssemblyAllele length
hg38189194
hg19189194
hg18189194
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3695253
Samples
Known GenesFNBP1, GPR107, NCS1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1046307
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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