A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1276n54



Internal ID20134700
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:79242612..79243739hg38UCSC Ensembl
chr10:81002369..81003496hg19UCSC Ensembl
chr10:80672375..80673502hg18UCSC Ensembl
Cytoband10q22.3
Allele length
AssemblyAllele length
hg381128
hg191128
hg181128
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv551581, nsv551585, nsv551577
Samples
Known GenesZMIZ1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv1276n54
Frequency
Sample Size17421
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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