A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1043941



Internal ID18786472
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:46455128..46489856hg38UCSC Ensembl
Innerchr10:47058780..47094632hg19UCSC Ensembl
Innerchr10:46478786..46514638hg18UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg3834729
hg1935853
hg1835853
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv811n100
Supporting Variantsnssv3705849
Samples
Known GenesLOC100996758, NPY4R
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1043941
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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