A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1045212



Internal ID19134431
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:117538312..117886082hg38UCSC Ensembl
Innerchr10:119297823..119645593hg19UCSC Ensembl
Innerchr10:119287813..119635583hg18UCSC Ensembl
Cytoband10q26.11
Allele length
AssemblyAllele length
hg38347771
hg19347771
hg18347771
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3508041
Samples
Known GenesEMX2, EMX2OS
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1045212
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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