A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv835n100



Internal ID20152451
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:46169941..46333389hg38UCSC Ensembl
chr10:47541177..47704625hg19UCSC Ensembl
chr10:47011183..47174631hg18UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg38163449
hg19163449
hg18163449
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1040102, nsv1048821, nsv1043598, nsv1053241, nsv1051217, nsv1050739, nsv1042540, nsv1039221, nsv1053149, nsv1039078, nsv1042838, nsv1048876, nsv1037302, nsv1043463, nsv1048673, nsv1046104, nsv1042521, nsv1050110, nsv1036741, nsv1046736, nsv1042546, nsv1049979, nsv1051204, nsv1052790, nsv1054373, nsv1051293, nsv1054181, nsv1052316, nsv1048105, nsv1039990, nsv1052112, nsv1043442, nsv1049446, nsv1042608, nsv1037103, nsv1043792, nsv1044232, nsv1051966, nsv1051375, nsv1053995, nsv1049208, nsv1045959
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)dgv835n100
Frequency
Sample Size29084
Observed Gain87
Observed Loss0
Observed Complex0
Frequencyn/a


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