A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv961n54



Internal ID20134385
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:14910793..15028616hg38UCSC Ensembl
chr10:14952792..15070615hg19UCSC Ensembl
chr10:14992798..15110621hg18UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg38117824
hg19117824
hg18117824
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv550001, nsv550000, nsv549999
Samples1782681109_A, 1780862043_A
Known GenesDCLRE1C, MEIG1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv961n54
Frequency
Sample Size17421
Observed Gain5
Observed Loss0
Observed Complex0
Frequencyn/a


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