A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv832n100



Internal ID20152448
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:46169941..46289800hg38UCSC Ensembl
chr10:47541177..47661036hg19UCSC Ensembl
chr10:47011183..47131042hg18UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg38119860
hg19119860
hg18119860
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1052433, nsv1048152, nsv1053502, nsv1048652, nsv1036342, nsv1050724, nsv1036150, nsv1039466, nsv1053082
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)dgv832n100
Frequency
Sample Size29084
Observed Gain59
Observed Loss100
Observed Complex0
Frequencyn/a


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