A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1015661



Internal ID18758195
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:7380008..7673246hg18UCSC Ensembl
Cytoband8p23.1
Allele length
AssemblyAllele length
hg18293239
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6946n100
Supporting Variantsnssv3680691
Samples
Known GenesFAM90A10P, FAM90A7P, PRR23D1, PRR23D2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1015661
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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