A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1039466



Internal ID18781997
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:46188877..46281567hg38UCSC Ensembl
Innerchr10:47560113..47652803hg19UCSC Ensembl
Innerchr10:47030119..47122809hg18UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg3892691
hg1992691
hg1892691
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv832n100
Supporting Variantsnssv3504680, nssv3706808
Samples
Known GenesANTXRLP1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1039466
Frequency
Sample Size29084
Observed Gain1
Observed Loss1
Observed Complex0
Frequencyn/a


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