A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv830n100



Internal ID20152446
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:46169941..46278156hg38UCSC Ensembl
chr10:47541177..47649392hg19UCSC Ensembl
chr10:47011183..47119398hg18UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg38108216
hg19108216
hg18108216
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1037490, nsv1046254, nsv1054118, nsv1048134, nsv1043526, nsv1045329, nsv1039207, nsv1038258, nsv1037651, nsv1045719
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)dgv830n100
Frequency
Sample Size29084
Observed Gain15
Observed Loss0
Observed Complex0
Frequencyn/a


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