A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv840n100



Internal ID20152456
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:46195678..46286428hg38UCSC Ensembl
chr10:47566914..47657664hg19UCSC Ensembl
chr10:47036920..47127670hg18UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg3890751
hg1990751
hg1890751
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1053485, nsv1052110, nsv1035345, nsv1046193, nsv1046443
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)dgv840n100
Frequency
Sample Size29084
Observed Gain6
Observed Loss0
Observed Complex0
Frequencyn/a


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