A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1050110



Internal ID18792641
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:46169941..46313699hg38UCSC Ensembl
Innerchr10:47541177..47684935hg19UCSC Ensembl
Innerchr10:47011183..47154941hg18UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg38143759
hg19143759
hg18143759
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv835n100
Supporting Variantsnssv3521526, nssv3506208, nssv3510424
Samples
Known GenesANTXRL, ANTXRLP1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1050110
Frequency
Sample Size29084
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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