A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv990n54



Internal ID22768885
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:20489512..20531900hg38UCSC Ensembl
chr10:20778441..20820829hg19UCSC Ensembl
chr10:20818447..20860835hg18UCSC Ensembl
Cytoband10p12.31
Allele length
AssemblyAllele length
hg3842389
hg1942389
hg1842389
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv550152, nsv550151, nsv550153, nsv550150
Samples1780862431_A
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv990n54
Frequency
Sample Size17421
Observed Gain7
Observed Loss0
Observed Complex0
Frequencyn/a


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