A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3512092



Internal ID18810373
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:68650726..68695174hg38UCSC Ensembl
Innerchr10:70410483..70454931hg19UCSC Ensembl
Innerchr10:70080489..70124937hg18UCSC Ensembl
Cytoband10q21.3
Allele length
AssemblyAllele length
hg3844449
hg1944449
hg1844449
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1049633
Supporting Variants
Samples
Known GenesTET1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3512092
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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