A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1110n54



Internal ID20134534
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:46166132..46393582hg38UCSC Ensembl
chr10:47537368..47764834hg19UCSC Ensembl
chr10:47007374..47234840hg18UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg38227451
hg19227467
hg18227467
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv550761, nsv550762, nsv550736, nsv550759, nsv550735
Samples
Known GenesANTXRL, ANTXRLP1, ANXA8L1, ANXA8L2, FAM25B
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv1110n54
Frequency
Sample Size17421
Observed Gain12
Observed Loss0
Observed Complex0
Frequencyn/a


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