A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1046186



Internal ID19135405
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:47020164..47109535hg19UCSC Ensembl
Innerchr10:46440170..46529541hg18UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg1989372
hg1889372
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv786n100
Supporting Variantsnssv3517838
Samples
Known GenesLINC00842, LOC100996758, NPY4R
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1046186
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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