A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1046666



Internal ID18789197
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:46961233..47108045hg19UCSC Ensembl
Innerchr10:46381239..46528051hg18UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg19146813
hg18146813
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv763n100
Supporting Variantsnssv3509122
Samples
Known GenesGPRIN2, LINC00842, LOC100996758, NPY4R, SYT15
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1046666
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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