A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv836n100



Internal ID20152452
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:46169941..46372244hg38UCSC Ensembl
chr10:47541177..47743504hg19UCSC Ensembl
chr10:47011183..47213510hg18UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg38202304
hg19202328
hg18202328
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1051110, nsv1038081, nsv1041131, nsv1054462
Samples
Known GenesANTXRL, ANTXRLP1, FAM25B
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv836n100
Frequency
Sample Size29084
Observed Gain85
Observed Loss8
Observed Complex0
Frequencyn/a


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